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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 08:46:16 UTC

Update Date

2021-09-26 23:03:24 UTC

HMDB ID

HMDB0251412

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Diminazene

Description

Diminazene belongs to the class of organic compounds known as phenylhydrazines. Phenylhydrazines are compounds containing a phenylhydrazide moiety, which consists of a hydrazide substituent attached to a phenyl group. Based on a literature review a significant number of articles have been published on Diminazene. This compound has been identified in human blood as reported by (PMID: 31557052 ). Diminazene is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Diminazene is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0251412
     RDKit          3D
Diminazene
 36 37  0  0  0  0  0  0  0  0999 V2000
   -6.7653    0.8661    1.8757 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3990    0.4414    0.7373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4013    0.0439   -0.1809 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0088    0.3556    0.3670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9888    0.7185    1.1995 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6669    0.6073    0.7749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3357    0.1383   -0.4720 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9836    0.0283   -0.8870 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1013   -0.6116   -0.5210 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9120   -1.3319   -0.1172 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3021   -0.9047   -0.0698 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1384   -1.1501   -1.1323 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4653   -0.7552   -1.1154 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0109   -0.0878   -0.0122 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4102    0.3100   -0.0310 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9945    0.9290    0.9302 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1980   -0.0030   -1.1866 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1607    0.1495    1.0408 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8173   -0.2506    1.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3569   -0.2275   -1.3120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6851   -0.1228   -0.9035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1470    1.1797    2.6191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8528   -0.8821   -0.0248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7258    0.5988   -0.9993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2054    1.0979    2.2025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8807    0.8963    1.4398 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7197   -2.3458    0.2179 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7305   -1.6659   -1.9940 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1291   -0.9446   -1.9444 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4649    1.1745    1.7856 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9899   -0.6726   -1.1253 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9948    0.4295   -2.1003 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5468    0.6674    1.9182 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1605   -0.0549    1.8646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1471   -0.6003   -2.2984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4942   -0.4126   -1.5689 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  3
 15 17  1  0
 14 18  1  0
 18 19  2  0
  7 20  1  0
 20 21  2  0
 21  4  1  0
 19 11  1  0
  1 22  1  0
  3 23  1  0
  3 24  1  0
  5 25  1  0
  6 26  1  0
 10 27  1  0
 12 28  1  0
 13 29  1  0
 16 30  1  0
 17 31  1  0
 17 32  1  0
 18 33  1  0
 19 34  1  0
 20 35  1  0
 21 36  1  0
M  END

BRN
  Mrv0541 02231217032D          

 21 22  0  0  0  0            999 V2000
   -1.2356   -0.8783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5211   -1.2908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5211   -2.1158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2356   -2.5283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9500   -2.1158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9500   -1.2908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2356   -3.3533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9500   -3.7658    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5211   -3.7658    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2356   -0.0533    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5211    0.3592    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5211    1.1842    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1934    1.5967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1934    2.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9078    2.8342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6223    2.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6223    1.5967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9078    1.1842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3368    2.8342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3368    3.6592    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0513    2.4217    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  6  1  0  0  0  0
  1 10  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  4  7  1  0  0  0  0
  5  6  2  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 18  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 19  1  0  0  0  0
 17 18  2  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0251412

> <DATABASE_NAME>
hmdb

> <SMILES>
NC(=N)C1=CC=C(N\N=N\C2=CC=C(C=C2)C(N)=N)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C14H15N7/c15-13(16)9-1-5-11(6-2-9)19-21-20-12-7-3-10(4-8-12)14(17)18/h1-8H,(H3,15,16)(H3,17,18)(H,19,20)

> <INCHI_KEY>
XNYZHCFCZNMTFY-UHFFFAOYSA-N

> <FORMULA>
C14H15N7

> <MOLECULAR_WEIGHT>
281.3158

> <EXACT_MASS>
281.138893515

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_AVERAGE_POLARIZABILITY>
30.173326192924193

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-[(2E)-3-(4-carbamimidoylphenyl)triaz-2-en-1-yl]benzene-1-carboximidamide

> <ALOGPS_LOGP>
1.09

> <JCHEM_LOGP>
1.7629520969999999

> <ALOGPS_LOGS>
-3.44

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.964028683768714

> <JCHEM_PKA_STRONGEST_BASIC>
12.068213952712284

> <JCHEM_POLAR_SURFACE_AREA>
136.49

> <JCHEM_REFRACTIVITY>
108.72829999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.02e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
diminazene

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0251412
     RDKit          3D
Diminazene
 36 37  0  0  0  0  0  0  0  0999 V2000
   -6.7653    0.8661    1.8757 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3990    0.4414    0.7373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4013    0.0439   -0.1809 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0088    0.3556    0.3670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9888    0.7185    1.1995 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6669    0.6073    0.7749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3357    0.1383   -0.4720 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9836    0.0283   -0.8870 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1013   -0.6116   -0.5210 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9120   -1.3319   -0.1172 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3021   -0.9047   -0.0698 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1384   -1.1501   -1.1323 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4653   -0.7552   -1.1154 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0109   -0.0878   -0.0122 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4102    0.3100   -0.0310 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9945    0.9290    0.9302 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1980   -0.0030   -1.1866 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1607    0.1495    1.0408 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8173   -0.2506    1.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3569   -0.2275   -1.3120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6851   -0.1228   -0.9035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1470    1.1797    2.6191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8528   -0.8821   -0.0248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7258    0.5988   -0.9993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2054    1.0979    2.2025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8807    0.8963    1.4398 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7197   -2.3458    0.2179 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7305   -1.6659   -1.9940 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1291   -0.9446   -1.9444 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4649    1.1745    1.7856 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9899   -0.6726   -1.1253 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9948    0.4295   -2.1003 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5468    0.6674    1.9182 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1605   -0.0549    1.8646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1471   -0.6003   -2.2984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4942   -0.4126   -1.5689 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  3
 15 17  1  0
 14 18  1  0
 18 19  2  0
  7 20  1  0
 20 21  2  0
 21  4  1  0
 19 11  1  0
  1 22  1  0
  3 23  1  0
  3 24  1  0
  5 25  1  0
  6 26  1  0
 10 27  1  0
 12 28  1  0
 13 29  1  0
 16 30  1  0
 17 31  1  0
 17 32  1  0
 18 33  1  0
 19 34  1  0
 20 35  1  0
 21 36  1  0
M  END

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: BRN                                               
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  C   UNK     0      -2.306  -1.639   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.973  -2.409   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.973  -3.949   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.306  -4.719   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.640  -3.949   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.640  -2.409   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.306  -6.259   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0      -3.640  -7.029   0.000  0.00  0.00           N+0
HETATM    9  N   UNK     0      -0.973  -7.029   0.000  0.00  0.00           N+0
HETATM   10  N   UNK     0      -2.306  -0.099   0.000  0.00  0.00           N+0
HETATM   11  N   UNK     0      -0.973   0.671   0.000  0.00  0.00           N+0
HETATM   12  N   UNK     0      -0.973   2.211   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       0.361   2.981   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.361   4.521   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.695   5.291   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.028   4.521   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.028   2.981   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.695   2.211   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.362   5.291   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       4.362   6.831   0.000  0.00  0.00           N+0
HETATM   21  N   UNK     0       5.696   4.521   0.000  0.00  0.00           N+0
CONECT    1    2    6   10                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    1    5                                                       
CONECT    7    4    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    1   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   13   17                                                       
CONECT   19   16   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

COMPND    HMDB0251412
HETATM    1  N1  UNL     1      -6.765   0.866   1.876  1.00  0.00           N  
HETATM    2  C1  UNL     1      -6.399   0.441   0.737  1.00  0.00           C  
HETATM    3  N2  UNL     1      -7.401   0.044  -0.181  1.00  0.00           N  
HETATM    4  C2  UNL     1      -5.009   0.356   0.367  1.00  0.00           C  
HETATM    5  C3  UNL     1      -3.989   0.718   1.199  1.00  0.00           C  
HETATM    6  C4  UNL     1      -2.667   0.607   0.775  1.00  0.00           C  
HETATM    7  C5  UNL     1      -2.336   0.138  -0.472  1.00  0.00           C  
HETATM    8  N3  UNL     1      -0.984   0.028  -0.887  1.00  0.00           N  
HETATM    9  N4  UNL     1      -0.101  -0.612  -0.521  1.00  0.00           N  
HETATM   10  N5  UNL     1       0.912  -1.332  -0.117  1.00  0.00           N  
HETATM   11  C6  UNL     1       2.302  -0.905  -0.070  1.00  0.00           C  
HETATM   12  C7  UNL     1       3.138  -1.150  -1.132  1.00  0.00           C  
HETATM   13  C8  UNL     1       4.465  -0.755  -1.115  1.00  0.00           C  
HETATM   14  C9  UNL     1       5.011  -0.088  -0.012  1.00  0.00           C  
HETATM   15  C10 UNL     1       6.410   0.310  -0.031  1.00  0.00           C  
HETATM   16  N6  UNL     1       6.995   0.929   0.930  1.00  0.00           N  
HETATM   17  N7  UNL     1       7.198  -0.003  -1.187  1.00  0.00           N  
HETATM   18  C11 UNL     1       4.161   0.149   1.041  1.00  0.00           C  
HETATM   19  C12 UNL     1       2.817  -0.251   1.023  1.00  0.00           C  
HETATM   20  C13 UNL     1      -3.357  -0.227  -1.312  1.00  0.00           C  
HETATM   21  C14 UNL     1      -4.685  -0.123  -0.903  1.00  0.00           C  
HETATM   22  H1  UNL     1      -6.147   1.180   2.619  1.00  0.00           H  
HETATM   23  H2  UNL     1      -7.853  -0.882  -0.025  1.00  0.00           H  
HETATM   24  H3  UNL     1      -7.726   0.599  -0.999  1.00  0.00           H  
HETATM   25  H4  UNL     1      -4.205   1.098   2.203  1.00  0.00           H  
HETATM   26  H5  UNL     1      -1.881   0.896   1.440  1.00  0.00           H  
HETATM   27  H6  UNL     1       0.720  -2.346   0.218  1.00  0.00           H  
HETATM   28  H7  UNL     1       2.731  -1.666  -1.994  1.00  0.00           H  
HETATM   29  H8  UNL     1       5.129  -0.945  -1.944  1.00  0.00           H  
HETATM   30  H9  UNL     1       6.465   1.174   1.786  1.00  0.00           H  
HETATM   31  H10 UNL     1       7.990  -0.673  -1.125  1.00  0.00           H  
HETATM   32  H11 UNL     1       6.995   0.429  -2.100  1.00  0.00           H  
HETATM   33  H12 UNL     1       4.547   0.667   1.918  1.00  0.00           H  
HETATM   34  H13 UNL     1       2.161  -0.055   1.865  1.00  0.00           H  
HETATM   35  H14 UNL     1      -3.147  -0.600  -2.298  1.00  0.00           H  
HETATM   36  H15 UNL     1      -5.494  -0.413  -1.569  1.00  0.00           H  
CONECT    1    2    2   22
CONECT    2    3    4
CONECT    3   23   24
CONECT    4    5    5   21
CONECT    5    6   25
CONECT    6    7    7   26
CONECT    7    8   20
CONECT    8    9    9
CONECT    9   10
CONECT   10   11   27
CONECT   11   12   12   19
CONECT   12   13   28
CONECT   13   14   14   29
CONECT   14   15   18
CONECT   15   16   16   17
CONECT   16   30
CONECT   17   31   32
CONECT   18   19   19   33
CONECT   19   34
CONECT   20   21   21   35
CONECT   21   36
END

HMDB0251412
     RDKit          3D
Diminazene
 36 37  0  0  0  0  0  0  0  0999 V2000
   -6.7653    0.8661    1.8757 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3990    0.4414    0.7373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4013    0.0439   -0.1809 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0088    0.3556    0.3670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9888    0.7185    1.1995 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6669    0.6073    0.7749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3357    0.1383   -0.4720 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9836    0.0283   -0.8870 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1013   -0.6116   -0.5210 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9120   -1.3319   -0.1172 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3021   -0.9047   -0.0698 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1384   -1.1501   -1.1323 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4653   -0.7552   -1.1154 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0109   -0.0878   -0.0122 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4102    0.3100   -0.0310 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9945    0.9290    0.9302 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1980   -0.0030   -1.1866 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1607    0.1495    1.0408 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8173   -0.2506    1.0232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3569   -0.2275   -1.3120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6851   -0.1228   -0.9035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1470    1.1797    2.6191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8528   -0.8821   -0.0248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7258    0.5988   -0.9993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2054    1.0979    2.2025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8807    0.8963    1.4398 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7197   -2.3458    0.2179 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7305   -1.6659   -1.9940 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1291   -0.9446   -1.9444 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4649    1.1745    1.7856 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9899   -0.6726   -1.1253 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9948    0.4295   -2.1003 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5468    0.6674    1.9182 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1605   -0.0549    1.8646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1471   -0.6003   -2.2984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4942   -0.4126   -1.5689 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  3
 15 17  1  0
 14 18  1  0
 18 19  2  0
  7 20  1  0
 20 21  2  0
 21  4  1  0
 19 11  1  0
  1 22  1  0
  3 23  1  0
  3 24  1  0
  5 25  1  0
  6 26  1  0
 10 27  1  0
 12 28  1  0
 13 29  1  0
 16 30  1  0
 17 31  1  0
 17 32  1  0
 18 33  1  0
 19 34  1  0
 20 35  1  0
 21 36  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
4,4'-(1-Triazene-1,3-diyl)bis-benzenecarboximidamide	ChEBI
Diminazeno	ChEBI
Diminazenum	ChEBI
4,4' Diazoaminobenzamidine	MeSH
4,4'-Diazoaminobenzamidine	MeSH

Chemical Formula

C₁₄H₁₅N₇

Average Molecular Weight

281.3158

Monoisotopic Molecular Weight

281.138893515

IUPAC Name

4-[(2E)-3-(4-carbamimidoylphenyl)triaz-2-en-1-yl]benzene-1-carboximidamide

Traditional Name

diminazene

CAS Registry Number

Not Available

SMILES

NC(=N)C1=CC=C(N\N=N\C2=CC=C(C=C2)C(N)=N)C=C1

InChI Identifier

InChI=1S/C14H15N7/c15-13(16)9-1-5-11(6-2-9)19-21-20-12-7-3-10(4-8-12)14(17)18/h1-8H,(H3,15,16)(H3,17,18)(H,19,20)

InChI Key

XNYZHCFCZNMTFY-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylhydrazines. Phenylhydrazines are compounds containing a phenylhydrazide moiety, which consists of a hydrazide substituent attached to a phenyl group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Phenylhydrazines

Direct Parent

Phenylhydrazines

Alternative Parents

Substituents

Phenylhydrazine
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carboximidamide
Carboxylic acid amidine
Amidine
Organic nitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Organonitrogen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

carboxamidine (CHEBI:81724 )
triazene derivative (CHEBI:81724 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	1.09	ALOGPS
logP	1.76	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	18.96	ChemAxon
pKa (Strongest Basic)	12.07	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	136.49 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	108.73 m³·mol⁻¹	ChemAxon
Polarizability	30.17 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	169.276	30932474
DeepCCS	[M-H]-	166.918	30932474
DeepCCS	[M-2H]-	200.826	30932474
DeepCCS	[M+Na]+	176.053	30932474
AllCCS	[M+H]+	166.2	32859911
AllCCS	[M+H-H2O]+	162.7	32859911
AllCCS	[M+NH4]+	169.4	32859911
AllCCS	[M+Na]+	170.3	32859911
AllCCS	[M-H]-	169.3	32859911
AllCCS	[M+Na-2H]-	168.9	32859911
AllCCS	[M+HCOO]-	168.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Diminazene	NC(=N)C1=CC=C(N\N=N\C2=CC=C(C=C2)C(N)=N)C=C1	4448.2	Standard polar	33892256
Diminazene	NC(=N)C1=CC=C(N\N=N\C2=CC=C(C=C2)C(N)=N)C=C1	3115.8	Standard non polar	33892256
Diminazene	NC(=N)C1=CC=C(N\N=N\C2=CC=C(C=C2)C(N)=N)C=C1	3683.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Diminazene,1TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	3746.6	Semi standard non polar	33892256
Diminazene,1TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	3161.3	Standard non polar	33892256
Diminazene,1TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	5652.5	Standard polar	33892256
Diminazene,1TMS,isomer #2	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	3752.4	Semi standard non polar	33892256
Diminazene,1TMS,isomer #2	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	3185.8	Standard non polar	33892256
Diminazene,1TMS,isomer #2	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	5652.6	Standard polar	33892256
Diminazene,1TMS,isomer #3	C[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	3697.9	Semi standard non polar	33892256
Diminazene,1TMS,isomer #3	C[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	3162.7	Standard non polar	33892256
Diminazene,1TMS,isomer #3	C[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	5620.2	Standard polar	33892256
Diminazene,1TMS,isomer #4	C[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N)C=C1)C1=CC=C(C(=N)N)C=C1	3529.1	Semi standard non polar	33892256
Diminazene,1TMS,isomer #4	C[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N)C=C1)C1=CC=C(C(=N)N)C=C1	3096.2	Standard non polar	33892256
Diminazene,1TMS,isomer #4	C[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N)C=C1)C1=CC=C(C(=N)N)C=C1	5741.1	Standard polar	33892256
Diminazene,1TMS,isomer #5	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	3694.4	Semi standard non polar	33892256
Diminazene,1TMS,isomer #5	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	3172.4	Standard non polar	33892256
Diminazene,1TMS,isomer #5	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	5620.0	Standard polar	33892256
Diminazene,2TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1	3856.4	Semi standard non polar	33892256
Diminazene,2TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1	3239.9	Standard non polar	33892256
Diminazene,2TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1	5166.7	Standard polar	33892256
Diminazene,2TMS,isomer #10	C[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	3574.7	Semi standard non polar	33892256
Diminazene,2TMS,isomer #10	C[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	3196.0	Standard non polar	33892256
Diminazene,2TMS,isomer #10	C[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	5353.9	Standard polar	33892256
Diminazene,2TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(N)=N[Si](C)(C)C)C=C2)C=C1	3740.1	Semi standard non polar	33892256
Diminazene,2TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(N)=N[Si](C)(C)C)C=C2)C=C1	3216.1	Standard non polar	33892256
Diminazene,2TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(N)=N[Si](C)(C)C)C=C2)C=C1	5355.2	Standard polar	33892256
Diminazene,2TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	3578.0	Semi standard non polar	33892256
Diminazene,2TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	3188.4	Standard non polar	33892256
Diminazene,2TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	5353.6	Standard polar	33892256
Diminazene,2TMS,isomer #2	C[Si](C)(C)N(C(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1)[Si](C)(C)C	3836.9	Semi standard non polar	33892256
Diminazene,2TMS,isomer #2	C[Si](C)(C)N(C(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1)[Si](C)(C)C	3138.9	Standard non polar	33892256
Diminazene,2TMS,isomer #2	C[Si](C)(C)N(C(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1)[Si](C)(C)C	5371.6	Standard polar	33892256
Diminazene,2TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	3735.8	Semi standard non polar	33892256
Diminazene,2TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	3159.2	Standard non polar	33892256
Diminazene,2TMS,isomer #3	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	5196.4	Standard polar	33892256
Diminazene,2TMS,isomer #4	C[Si](C)(C)NC(=N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	3679.8	Semi standard non polar	33892256
Diminazene,2TMS,isomer #4	C[Si](C)(C)NC(=N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	3195.3	Standard non polar	33892256
Diminazene,2TMS,isomer #4	C[Si](C)(C)NC(=N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	5213.0	Standard polar	33892256
Diminazene,2TMS,isomer #5	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1	3826.9	Semi standard non polar	33892256
Diminazene,2TMS,isomer #5	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1	3263.0	Standard non polar	33892256
Diminazene,2TMS,isomer #5	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1	5263.4	Standard polar	33892256
Diminazene,2TMS,isomer #6	C[Si](C)(C)N(C(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1)[Si](C)(C)C	3834.7	Semi standard non polar	33892256
Diminazene,2TMS,isomer #6	C[Si](C)(C)N(C(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1)[Si](C)(C)C	3142.9	Standard non polar	33892256
Diminazene,2TMS,isomer #6	C[Si](C)(C)N(C(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1)[Si](C)(C)C	5372.1	Standard polar	33892256
Diminazene,2TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	3725.4	Semi standard non polar	33892256
Diminazene,2TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	3180.7	Standard non polar	33892256
Diminazene,2TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	5195.4	Standard polar	33892256
Diminazene,2TMS,isomer #8	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	3682.8	Semi standard non polar	33892256
Diminazene,2TMS,isomer #8	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	3169.7	Standard non polar	33892256
Diminazene,2TMS,isomer #8	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	5216.6	Standard polar	33892256
Diminazene,2TMS,isomer #9	C[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1	3827.0	Semi standard non polar	33892256
Diminazene,2TMS,isomer #9	C[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1	3261.1	Standard non polar	33892256
Diminazene,2TMS,isomer #9	C[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1	5263.7	Standard polar	33892256
Diminazene,3TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3873.1	Semi standard non polar	33892256
Diminazene,3TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3242.6	Standard non polar	33892256
Diminazene,3TMS,isomer #1	C[Si](C)(C)NC(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	4872.8	Standard polar	33892256
Diminazene,3TMS,isomer #10	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)C=C1	3657.6	Semi standard non polar	33892256
Diminazene,3TMS,isomer #10	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)C=C1	3268.7	Standard non polar	33892256
Diminazene,3TMS,isomer #10	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)C=C1	4987.0	Standard polar	33892256
Diminazene,3TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3634.8	Semi standard non polar	33892256
Diminazene,3TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3265.7	Standard non polar	33892256
Diminazene,3TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	4992.4	Standard polar	33892256
Diminazene,3TMS,isomer #12	C[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3743.3	Semi standard non polar	33892256
Diminazene,3TMS,isomer #12	C[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3206.9	Standard non polar	33892256
Diminazene,3TMS,isomer #12	C[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4852.2	Standard polar	33892256
Diminazene,3TMS,isomer #13	C[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1)C1=CC=C(C(=N)N)C=C1	3622.4	Semi standard non polar	33892256
Diminazene,3TMS,isomer #13	C[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1)C1=CC=C(C(=N)N)C=C1	3194.7	Standard non polar	33892256
Diminazene,3TMS,isomer #13	C[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1)C1=CC=C(C(=N)N)C=C1	4963.4	Standard polar	33892256
Diminazene,3TMS,isomer #14	C[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3749.5	Semi standard non polar	33892256
Diminazene,3TMS,isomer #14	C[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3269.4	Standard non polar	33892256
Diminazene,3TMS,isomer #14	C[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	5101.7	Standard polar	33892256
Diminazene,3TMS,isomer #15	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	3534.5	Semi standard non polar	33892256
Diminazene,3TMS,isomer #15	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	3162.0	Standard non polar	33892256
Diminazene,3TMS,isomer #15	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	4847.2	Standard polar	33892256
Diminazene,3TMS,isomer #16	C[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)C=C1	3657.2	Semi standard non polar	33892256
Diminazene,3TMS,isomer #16	C[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)C=C1	3272.7	Standard non polar	33892256
Diminazene,3TMS,isomer #16	C[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)C=C1	4986.1	Standard polar	33892256
Diminazene,3TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3635.7	Semi standard non polar	33892256
Diminazene,3TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3249.8	Standard non polar	33892256
Diminazene,3TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	4996.3	Standard polar	33892256
Diminazene,3TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(N)=N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3524.2	Semi standard non polar	33892256
Diminazene,3TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(N)=N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3216.4	Standard non polar	33892256
Diminazene,3TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(N)=N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	5214.2	Standard polar	33892256
Diminazene,3TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1	3763.9	Semi standard non polar	33892256
Diminazene,3TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1	3276.4	Standard non polar	33892256
Diminazene,3TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1	4786.8	Standard polar	33892256
Diminazene,3TMS,isomer #3	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3701.8	Semi standard non polar	33892256
Diminazene,3TMS,isomer #3	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3245.8	Standard non polar	33892256
Diminazene,3TMS,isomer #3	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	4730.9	Standard polar	33892256
Diminazene,3TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1	3761.3	Semi standard non polar	33892256
Diminazene,3TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1	3279.8	Standard non polar	33892256
Diminazene,3TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1	4788.2	Standard polar	33892256
Diminazene,3TMS,isomer #5	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3872.1	Semi standard non polar	33892256
Diminazene,3TMS,isomer #5	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3260.5	Standard non polar	33892256
Diminazene,3TMS,isomer #5	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	4871.8	Standard polar	33892256
Diminazene,3TMS,isomer #6	C[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3755.4	Semi standard non polar	33892256
Diminazene,3TMS,isomer #6	C[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3207.2	Standard non polar	33892256
Diminazene,3TMS,isomer #6	C[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4852.5	Standard polar	33892256
Diminazene,3TMS,isomer #7	C[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N)C=C1)C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1	3620.6	Semi standard non polar	33892256
Diminazene,3TMS,isomer #7	C[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N)C=C1)C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1	3187.6	Standard non polar	33892256
Diminazene,3TMS,isomer #7	C[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N)C=C1)C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1	4960.7	Standard polar	33892256
Diminazene,3TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3753.0	Semi standard non polar	33892256
Diminazene,3TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3267.9	Standard non polar	33892256
Diminazene,3TMS,isomer #8	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	5100.8	Standard polar	33892256
Diminazene,3TMS,isomer #9	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	3539.2	Semi standard non polar	33892256
Diminazene,3TMS,isomer #9	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	3173.2	Standard non polar	33892256
Diminazene,3TMS,isomer #9	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1	4842.3	Standard polar	33892256
Diminazene,4TMS,isomer #1	C[Si](C)(C)N(C(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1)[Si](C)(C)C	3782.1	Semi standard non polar	33892256
Diminazene,4TMS,isomer #1	C[Si](C)(C)N(C(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1)[Si](C)(C)C	3333.1	Standard non polar	33892256
Diminazene,4TMS,isomer #1	C[Si](C)(C)N(C(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1)[Si](C)(C)C	4639.6	Standard polar	33892256
Diminazene,4TMS,isomer #10	C[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3744.3	Semi standard non polar	33892256
Diminazene,4TMS,isomer #10	C[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3316.4	Standard non polar	33892256
Diminazene,4TMS,isomer #10	C[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4414.7	Standard polar	33892256
Diminazene,4TMS,isomer #11	C[Si](C)(C)N=C(C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3508.4	Semi standard non polar	33892256
Diminazene,4TMS,isomer #11	C[Si](C)(C)N=C(C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3189.1	Standard non polar	33892256
Diminazene,4TMS,isomer #11	C[Si](C)(C)N=C(C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4527.7	Standard polar	33892256
Diminazene,4TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3635.6	Semi standard non polar	33892256
Diminazene,4TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3308.5	Standard non polar	33892256
Diminazene,4TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	4732.6	Standard polar	33892256
Diminazene,4TMS,isomer #13	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3559.5	Semi standard non polar	33892256
Diminazene,4TMS,isomer #13	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3261.3	Standard non polar	33892256
Diminazene,4TMS,isomer #13	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	4832.7	Standard polar	33892256
Diminazene,4TMS,isomer #14	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3498.7	Semi standard non polar	33892256
Diminazene,4TMS,isomer #14	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3213.3	Standard non polar	33892256
Diminazene,4TMS,isomer #14	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	4751.6	Standard polar	33892256
Diminazene,4TMS,isomer #15	C[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3509.3	Semi standard non polar	33892256
Diminazene,4TMS,isomer #15	C[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3180.9	Standard non polar	33892256
Diminazene,4TMS,isomer #15	C[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4533.5	Standard polar	33892256
Diminazene,4TMS,isomer #16	C[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3638.2	Semi standard non polar	33892256
Diminazene,4TMS,isomer #16	C[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3308.3	Standard non polar	33892256
Diminazene,4TMS,isomer #16	C[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	4732.5	Standard polar	33892256
Diminazene,4TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3555.9	Semi standard non polar	33892256
Diminazene,4TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3268.3	Standard non polar	33892256
Diminazene,4TMS,isomer #17	C[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	4835.7	Standard polar	33892256
Diminazene,4TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3498.1	Semi standard non polar	33892256
Diminazene,4TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3216.0	Standard non polar	33892256
Diminazene,4TMS,isomer #18	C[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	4756.5	Standard polar	33892256
Diminazene,4TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3707.2	Semi standard non polar	33892256
Diminazene,4TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3294.6	Standard non polar	33892256
Diminazene,4TMS,isomer #2	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	4563.5	Standard polar	33892256
Diminazene,4TMS,isomer #3	C[Si](C)(C)NC(=N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3642.2	Semi standard non polar	33892256
Diminazene,4TMS,isomer #3	C[Si](C)(C)NC(=N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3266.0	Standard non polar	33892256
Diminazene,4TMS,isomer #3	C[Si](C)(C)NC(=N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	4495.2	Standard polar	33892256
Diminazene,4TMS,isomer #4	C[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3748.5	Semi standard non polar	33892256
Diminazene,4TMS,isomer #4	C[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3307.1	Standard non polar	33892256
Diminazene,4TMS,isomer #4	C[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4414.7	Standard polar	33892256
Diminazene,4TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3593.5	Semi standard non polar	33892256
Diminazene,4TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3235.8	Standard non polar	33892256
Diminazene,4TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	4438.7	Standard polar	33892256
Diminazene,4TMS,isomer #6	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)C=C1	3663.1	Semi standard non polar	33892256
Diminazene,4TMS,isomer #6	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)C=C1	3299.0	Standard non polar	33892256
Diminazene,4TMS,isomer #6	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)C=C1	4506.5	Standard polar	33892256
Diminazene,4TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3706.5	Semi standard non polar	33892256
Diminazene,4TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3292.3	Standard non polar	33892256
Diminazene,4TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	4561.4	Standard polar	33892256
Diminazene,4TMS,isomer #8	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3596.9	Semi standard non polar	33892256
Diminazene,4TMS,isomer #8	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3229.7	Standard non polar	33892256
Diminazene,4TMS,isomer #8	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	4438.2	Standard polar	33892256
Diminazene,4TMS,isomer #9	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3642.3	Semi standard non polar	33892256
Diminazene,4TMS,isomer #9	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3255.5	Standard non polar	33892256
Diminazene,4TMS,isomer #9	C[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	4496.2	Standard polar	33892256
Diminazene,5TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3673.2	Semi standard non polar	33892256
Diminazene,5TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3346.9	Standard non polar	33892256
Diminazene,5TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4238.9	Standard polar	33892256
Diminazene,5TMS,isomer #10	C[Si](C)(C)N=C(C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3559.6	Semi standard non polar	33892256
Diminazene,5TMS,isomer #10	C[Si](C)(C)N=C(C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3252.0	Standard non polar	33892256
Diminazene,5TMS,isomer #10	C[Si](C)(C)N=C(C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4117.5	Standard polar	33892256
Diminazene,5TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3488.5	Semi standard non polar	33892256
Diminazene,5TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3236.2	Standard non polar	33892256
Diminazene,5TMS,isomer #11	C[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	4518.1	Standard polar	33892256
Diminazene,5TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3488.2	Semi standard non polar	33892256
Diminazene,5TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3234.7	Standard non polar	33892256
Diminazene,5TMS,isomer #12	C[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	4524.0	Standard polar	33892256
Diminazene,5TMS,isomer #2	C[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1)C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1	3613.2	Semi standard non polar	33892256
Diminazene,5TMS,isomer #2	C[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1)C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1	3312.8	Standard non polar	33892256
Diminazene,5TMS,isomer #2	C[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1)C1=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C1	4326.7	Standard polar	33892256
Diminazene,5TMS,isomer #3	C[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3670.8	Semi standard non polar	33892256
Diminazene,5TMS,isomer #3	C[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3343.7	Standard non polar	33892256
Diminazene,5TMS,isomer #3	C[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4239.2	Standard polar	33892256
Diminazene,5TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3552.7	Semi standard non polar	33892256
Diminazene,5TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3237.8	Standard non polar	33892256
Diminazene,5TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	4275.0	Standard polar	33892256
Diminazene,5TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3628.0	Semi standard non polar	33892256
Diminazene,5TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3331.8	Standard non polar	33892256
Diminazene,5TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	4198.1	Standard polar	33892256
Diminazene,5TMS,isomer #6	C[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3560.8	Semi standard non polar	33892256
Diminazene,5TMS,isomer #6	C[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3252.0	Standard non polar	33892256
Diminazene,5TMS,isomer #6	C[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4119.6	Standard polar	33892256
Diminazene,5TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3529.1	Semi standard non polar	33892256
Diminazene,5TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3212.9	Standard non polar	33892256
Diminazene,5TMS,isomer #7	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C)N[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	4230.6	Standard polar	33892256
Diminazene,5TMS,isomer #8	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3555.7	Semi standard non polar	33892256
Diminazene,5TMS,isomer #8	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3235.1	Standard non polar	33892256
Diminazene,5TMS,isomer #8	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	4276.1	Standard polar	33892256
Diminazene,5TMS,isomer #9	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3625.2	Semi standard non polar	33892256
Diminazene,5TMS,isomer #9	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	3325.0	Standard non polar	33892256
Diminazene,5TMS,isomer #9	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1	4195.8	Standard polar	33892256
Diminazene,6TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3557.7	Semi standard non polar	33892256
Diminazene,6TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3274.1	Standard non polar	33892256
Diminazene,6TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4002.7	Standard polar	33892256
Diminazene,6TMS,isomer #2	C[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3597.9	Semi standard non polar	33892256
Diminazene,6TMS,isomer #2	C[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3391.0	Standard non polar	33892256
Diminazene,6TMS,isomer #2	C[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3919.5	Standard polar	33892256
Diminazene,6TMS,isomer #3	C[Si](C)(C)N=C(C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3556.7	Semi standard non polar	33892256
Diminazene,6TMS,isomer #3	C[Si](C)(C)N=C(C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3272.0	Standard non polar	33892256
Diminazene,6TMS,isomer #3	C[Si](C)(C)N=C(C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	4000.1	Standard polar	33892256
Diminazene,6TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3502.2	Semi standard non polar	33892256
Diminazene,6TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3244.0	Standard non polar	33892256
Diminazene,6TMS,isomer #4	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3961.6	Standard polar	33892256
Diminazene,6TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3503.7	Semi standard non polar	33892256
Diminazene,6TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3245.0	Standard non polar	33892256
Diminazene,6TMS,isomer #5	C[Si](C)(C)N=C(N[Si](C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1	3960.0	Standard polar	33892256
Diminazene,7TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3529.8	Semi standard non polar	33892256
Diminazene,7TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3287.6	Standard non polar	33892256
Diminazene,7TMS,isomer #1	C[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C	3741.2	Standard polar	33892256
Diminazene,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	4016.7	Semi standard non polar	33892256
Diminazene,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	3285.2	Standard non polar	33892256
Diminazene,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	5442.2	Standard polar	33892256
Diminazene,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	4019.1	Semi standard non polar	33892256
Diminazene,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	3308.5	Standard non polar	33892256
Diminazene,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	5442.6	Standard polar	33892256
Diminazene,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	3952.0	Semi standard non polar	33892256
Diminazene,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	3301.7	Standard non polar	33892256
Diminazene,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	5498.8	Standard polar	33892256
Diminazene,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N)C=C1)C1=CC=C(C(=N)N)C=C1	3807.5	Semi standard non polar	33892256
Diminazene,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N)C=C1)C1=CC=C(C(=N)N)C=C1	3232.7	Standard non polar	33892256
Diminazene,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N)C=C1)C1=CC=C(C(=N)N)C=C1	5560.7	Standard polar	33892256
Diminazene,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	3945.7	Semi standard non polar	33892256
Diminazene,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	3315.8	Standard non polar	33892256
Diminazene,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	5498.8	Standard polar	33892256
Diminazene,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	4431.8	Semi standard non polar	33892256
Diminazene,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	3564.2	Standard non polar	33892256
Diminazene,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	4877.8	Standard polar	33892256
Diminazene,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4071.0	Semi standard non polar	33892256
Diminazene,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3512.8	Standard non polar	33892256
Diminazene,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	5198.2	Standard polar	33892256
Diminazene,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C2)C=C1	4237.7	Semi standard non polar	33892256
Diminazene,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C2)C=C1	3548.8	Standard non polar	33892256
Diminazene,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C2)C=C1	5268.5	Standard polar	33892256
Diminazene,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4071.4	Semi standard non polar	33892256
Diminazene,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3506.0	Standard non polar	33892256
Diminazene,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	5198.1	Standard polar	33892256
Diminazene,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1)[Si](C)(C)C(C)(C)C	4326.4	Semi standard non polar	33892256
Diminazene,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1)[Si](C)(C)C(C)(C)C	3473.4	Standard non polar	33892256
Diminazene,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1)[Si](C)(C)C(C)(C)C	5102.1	Standard polar	33892256
Diminazene,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	4245.0	Semi standard non polar	33892256
Diminazene,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	3515.9	Standard non polar	33892256
Diminazene,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1	4976.0	Standard polar	33892256
Diminazene,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4187.7	Semi standard non polar	33892256
Diminazene,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3533.5	Standard non polar	33892256
Diminazene,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4944.7	Standard polar	33892256
Diminazene,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	4346.6	Semi standard non polar	33892256
Diminazene,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	3575.2	Standard non polar	33892256
Diminazene,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	5077.9	Standard polar	33892256
Diminazene,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1)[Si](C)(C)C(C)(C)C	4316.8	Semi standard non polar	33892256
Diminazene,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1)[Si](C)(C)C(C)(C)C	3469.8	Standard non polar	33892256
Diminazene,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1)[Si](C)(C)C(C)(C)C	5102.7	Standard polar	33892256
Diminazene,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	4231.6	Semi standard non polar	33892256
Diminazene,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	3526.4	Standard non polar	33892256
Diminazene,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1	4974.9	Standard polar	33892256
Diminazene,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4189.6	Semi standard non polar	33892256
Diminazene,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3510.5	Standard non polar	33892256
Diminazene,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4948.9	Standard polar	33892256
Diminazene,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	4348.6	Semi standard non polar	33892256
Diminazene,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	3581.1	Standard non polar	33892256
Diminazene,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	5077.8	Standard polar	33892256
Diminazene,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4522.2	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	3784.9	Standard non polar	33892256
Diminazene,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4653.1	Standard polar	33892256
Diminazene,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	4301.8	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	3788.7	Standard non polar	33892256
Diminazene,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	4895.0	Standard polar	33892256
Diminazene,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4307.6	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3749.1	Standard non polar	33892256
Diminazene,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4847.0	Standard polar	33892256
Diminazene,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4308.9	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3739.2	Standard non polar	33892256
Diminazene,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4700.6	Standard polar	33892256
Diminazene,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)C1=CC=C(C(=N)N)C=C1	4213.2	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)C1=CC=C(C(=N)N)C=C1	3659.3	Standard non polar	33892256
Diminazene,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)C1=CC=C(C(=N)N)C=C1	4748.6	Standard polar	33892256
Diminazene,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4415.9	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	3791.6	Standard non polar	33892256
Diminazene,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4934.8	Standard polar	33892256
Diminazene,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4155.6	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3646.8	Standard non polar	33892256
Diminazene,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4716.0	Standard polar	33892256
Diminazene,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	4301.5	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	3790.5	Standard non polar	33892256
Diminazene,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	4893.4	Standard polar	33892256
Diminazene,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4298.7	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3748.8	Standard non polar	33892256
Diminazene,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4851.1	Standard polar	33892256
Diminazene,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4197.2	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3700.5	Standard non polar	33892256
Diminazene,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(N)=N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	5141.1	Standard polar	33892256
Diminazene,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	4428.3	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	3809.2	Standard non polar	33892256
Diminazene,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	4613.1	Standard polar	33892256
Diminazene,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4414.6	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3765.8	Standard non polar	33892256
Diminazene,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4541.5	Standard polar	33892256
Diminazene,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	4433.7	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	3828.7	Standard non polar	33892256
Diminazene,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	4614.9	Standard polar	33892256
Diminazene,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4530.7	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	3799.5	Standard non polar	33892256
Diminazene,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4652.9	Standard polar	33892256
Diminazene,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4314.7	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3735.1	Standard non polar	33892256
Diminazene,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4701.4	Standard polar	33892256
Diminazene,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N)C=C1)C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	4221.5	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N)C=C1)C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	3660.1	Standard non polar	33892256
Diminazene,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N)C=C1)C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	4745.2	Standard polar	33892256
Diminazene,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4417.5	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	3787.9	Standard non polar	33892256
Diminazene,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4934.7	Standard polar	33892256
Diminazene,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4161.5	Semi standard non polar	33892256
Diminazene,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3658.5	Standard non polar	33892256
Diminazene,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4711.1	Standard polar	33892256
Diminazene,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1)[Si](C)(C)C(C)(C)C	4524.9	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1)[Si](C)(C)C(C)(C)C	3974.1	Standard non polar	33892256
Diminazene,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N(C(=N)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1)[Si](C)(C)C(C)(C)C	4500.1	Standard polar	33892256
Diminazene,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4467.8	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3985.7	Standard non polar	33892256
Diminazene,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4375.8	Standard polar	33892256
Diminazene,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4253.5	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3776.9	Standard non polar	33892256
Diminazene,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(N(/N=N/C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4513.6	Standard polar	33892256
Diminazene,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4394.7	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	3961.9	Standard non polar	33892256
Diminazene,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4712.5	Standard polar	33892256
Diminazene,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4338.6	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3841.1	Standard non polar	33892256
Diminazene,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4761.1	Standard polar	33892256
Diminazene,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4269.4	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3808.3	Standard non polar	33892256
Diminazene,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4738.9	Standard polar	33892256
Diminazene,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4250.5	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3772.6	Standard non polar	33892256
Diminazene,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N)N)C=C2)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4519.3	Standard polar	33892256
Diminazene,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4393.2	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	3959.1	Standard non polar	33892256
Diminazene,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4712.2	Standard polar	33892256
Diminazene,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4335.6	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3845.3	Standard non polar	33892256
Diminazene,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4764.7	Standard polar	33892256
Diminazene,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4266.0	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3805.3	Standard non polar	33892256
Diminazene,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4743.8	Standard polar	33892256
Diminazene,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4436.6	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	3962.7	Standard non polar	33892256
Diminazene,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4486.7	Standard polar	33892256
Diminazene,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4390.4	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3881.0	Standard non polar	33892256
Diminazene,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4408.8	Standard polar	33892256
Diminazene,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4463.9	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3976.6	Standard non polar	33892256
Diminazene,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4376.4	Standard polar	33892256
Diminazene,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4321.7	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3850.1	Standard non polar	33892256
Diminazene,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4395.8	Standard polar	33892256
Diminazene,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	4314.3	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	3978.0	Standard non polar	33892256
Diminazene,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)C=C1	4472.1	Standard polar	33892256
Diminazene,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4436.6	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	3961.7	Standard non polar	33892256
Diminazene,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4484.5	Standard polar	33892256
Diminazene,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4326.3	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3855.0	Standard non polar	33892256
Diminazene,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4395.1	Standard polar	33892256
Diminazene,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4394.1	Semi standard non polar	33892256
Diminazene,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3878.2	Standard non polar	33892256
Diminazene,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC(=N)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4409.3	Standard polar	33892256
Diminazene,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4523.4	Semi standard non polar	33892256
Diminazene,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4102.8	Standard non polar	33892256
Diminazene,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/N=N/NC2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4296.0	Standard polar	33892256
Diminazene,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4422.4	Semi standard non polar	33892256
Diminazene,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3982.9	Standard non polar	33892256
Diminazene,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(N(/N=N/C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4235.9	Standard polar	33892256
Diminazene,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4401.3	Semi standard non polar	33892256
Diminazene,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3942.9	Standard non polar	33892256
Diminazene,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4610.8	Standard polar	33892256
Diminazene,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4404.2	Semi standard non polar	33892256
Diminazene,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3941.1	Standard non polar	33892256
Diminazene,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N=C(N)C1=CC=C(N(/N=N/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4615.9	Standard polar	33892256
Diminazene,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	4432.9	Semi standard non polar	33892256
Diminazene,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	4039.4	Standard non polar	33892256
Diminazene,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(/N=N/C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1)C1=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1	4310.0	Standard polar	33892256
Diminazene,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4526.9	Semi standard non polar	33892256
Diminazene,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4103.8	Standard non polar	33892256
Diminazene,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(N/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4295.8	Standard polar	33892256
Diminazene,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4376.9	Semi standard non polar	33892256
Diminazene,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3964.2	Standard non polar	33892256
Diminazene,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N(/N=N/C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4331.3	Standard polar	33892256
Diminazene,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4447.1	Semi standard non polar	33892256
Diminazene,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4104.0	Standard non polar	33892256
Diminazene,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(N/N=N/C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4313.4	Standard polar	33892256
Diminazene,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4420.7	Semi standard non polar	33892256
Diminazene,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3982.2	Standard non polar	33892256
Diminazene,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N=C(C1=CC=C(/N=N/N(C2=CC=C(C(=N)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4237.7	Standard polar	33892256
Diminazene,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4285.3	Semi standard non polar	33892256
Diminazene,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3948.5	Standard non polar	33892256
Diminazene,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4341.4	Standard polar	33892256
Diminazene,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4377.2	Semi standard non polar	33892256
Diminazene,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	3959.8	Standard non polar	33892256
Diminazene,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/N(C2=CC=C(C(=N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)C=C1	4331.8	Standard polar	33892256
Diminazene,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4443.3	Semi standard non polar	33892256
Diminazene,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4111.0	Standard non polar	33892256
Diminazene,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N=C(N[Si](C)(C)C(C)(C)C)C1=CC=C(/N=N/NC2=CC=C(C(=N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C2)C=C1	4310.9	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Diminazene GC-MS (Non-derivatized) - 70eV, Positive	splash10-00ll-4890000000-6c6ad84e2572cc7692f1	2017-08-28	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Diminazene GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Diminazene 10V, Positive-QTOF	splash10-001i-0090000000-10d8d7bd5eca683046e3	2017-07-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Diminazene 20V, Positive-QTOF	splash10-00lr-0090000000-ec6e9a26bb2a81885bd7	2017-07-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Diminazene 40V, Positive-QTOF	splash10-0aou-6790000000-8dcb2c1177aba2e0da30	2017-07-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Diminazene 10V, Negative-QTOF	splash10-001i-0090000000-f6698f4e537d3940e231	2017-07-26	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Diminazene 20V, Negative-QTOF	splash10-001i-0090000000-e0a2df7789a71578f4da	2017-07-26	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Diminazene 40V, Negative-QTOF	splash10-0006-9180000000-b57eb56df82c720bb793	2017-07-26	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Diminazene 10V, Positive-QTOF	splash10-001i-0090000000-a80f9ec9bbc23b21675d	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Diminazene 20V, Positive-QTOF	splash10-001i-0090000000-fe683c8ab4c9d471fe49	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Diminazene 40V, Positive-QTOF	splash10-0a4j-2930000000-b15de2da2b772d23f0e7	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Diminazene 10V, Negative-QTOF	splash10-001i-0090000000-ce408b0303b4fbcc6907	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Diminazene 20V, Negative-QTOF	splash10-001i-0090000000-4319c4d4071b38cd5e51	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Diminazene 40V, Negative-QTOF	splash10-0006-9600000000-48fa66eef26997fd95ad	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

DB03608

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

2264

KEGG Compound ID

C18388

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Diminazen

METLIN ID

Not Available

PubChem Compound

2354

PDB ID

Not Available

ChEBI ID

81724

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for Diminazene (HMDB0251412)

MOL for HMDB0251412 (Diminazene)

3D MOL for HMDB0251412 (Diminazene)

3D SDF for HMDB0251412 (Diminazene)

3D-SDF for HMDB0251412 (Diminazene)

PDB for HMDB0251412 (Diminazene)

3D PDB for HMDB0251412 (Diminazene)

SMILES for HMDB0251412 (Diminazene)

INCHI for HMDB0251412 (Diminazene)

Structure for HMDB0251412 (Diminazene)

3D Structure for HMDB0251412 (Diminazene)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra