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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 18:10:23 UTC

Update Date

2021-09-26 23:13:31 UTC

HMDB ID

HMDB0257269

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide

Description

4-chloro-N-[2-(4-oxo-4λ⁵-morpholin-4-yl)ethyl]benzamide belongs to the class of organic compounds known as 4-halobenzoic acids and derivatives. These are benzoic acids or derivatives carrying a halogen atom at the 4-position of the benzene ring. Based on a literature review very few articles have been published on 4-chloro-N-[2-(4-oxo-4λ⁵-morpholin-4-yl)ethyl]benzamide. This compound has been identified in human blood as reported by (PMID: 31557052 ). Benzamide, 4-chloro-n-(2-(4-morpholinyl)ethyl)-, n-oxide is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide 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

HMDB0257269
     RDKit          3D
Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide
 36 37  0  0  0  0  0  0  0  0999 V2000
   -1.9905   -1.6145   -1.4270 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1886   -0.6289   -0.6596 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0792   -0.0284   -0.0424 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2438   -0.5306   -0.2849 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3006    0.2534    0.4731 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5788   -0.3217    0.1667 N   0  0  0  0  0  4  0  0  0  0  0  0
    2.4629   -1.4575   -0.5737 O   0  0  0  0  0  1  0  0  0  0  0  0
    3.3695   -0.6403    1.3197 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6815    0.1070    1.3603 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4315   -0.0654    0.2051 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6682   -0.0578   -0.9483 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3373    0.6143   -0.6745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5644   -0.1610   -0.4511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8566    0.8925    0.3596 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1634    1.3369    0.5575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1654    0.6707   -0.0995 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8360    1.1567    0.0876 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -5.9044   -0.3957   -0.9243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6073   -0.7937   -1.0862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2091    0.7772    0.5887 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4284   -0.5062   -1.3708 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3414   -1.5962    0.0420 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0656    0.2490    1.5457 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2437    1.3042    0.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5695   -1.7460    1.4053 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8140   -0.3608    2.2413 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4819    1.1580    1.5818 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2795   -0.3185    2.1964 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4444   -1.1166   -1.2037 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1745    0.4386   -1.7989 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5035    1.5773   -0.1588 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7561    0.7503   -1.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0969    1.4428    0.8940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3778    2.1861    1.2136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7061   -0.9320   -1.4527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4309   -1.6436   -1.7475 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
  2 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 12  6  1  0
 19 13  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  8 25  1  0
  8 26  1  0
  9 27  1  0
  9 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
 12 32  1  0
 14 33  1  0
 15 34  1  0
 18 35  1  0
 19 36  1  0
M  CHG  2   6   1   7  -1
M  END


  Mrv1652309112120102D          

 19 20  0  0  0  0            999 V2000
   -0.8245   -2.5038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2617   -1.8042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8744   -1.0757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0499   -1.0469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3873   -1.7466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    0.0575   -3.2980    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 15 18  1  0  0  0  0
  6 19  1  0  0  0  0
M  CHG  2   6   1  19  -1
M  END
> <DATABASE_ID>
HMDB0257269

> <DATABASE_NAME>
hmdb

> <SMILES>
[O-][N+]1(CCNC(=O)C2=CC=C(Cl)C=C2)CCOCC1

> <INCHI_IDENTIFIER>
InChI=1S/C13H17ClN2O3/c14-12-3-1-11(2-4-12)13(17)15-5-6-16(18)7-9-19-10-8-16/h1-4H,5-10H2,(H,15,17)

> <INCHI_KEY>
CJTZZADPEGGIMM-UHFFFAOYSA-N

> <FORMULA>
C13H17ClN2O3

> <MOLECULAR_WEIGHT>
284.74

> <EXACT_MASS>
284.0927701

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
29.106297544789516

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-{2-[(4-chlorophenyl)formamido]ethyl}morpholin-4-ium-4-olate

> <ALOGPS_LOGP>
0.38

> <JCHEM_LOGP>
0.32737573966666667

> <ALOGPS_LOGS>
-3.51

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.660806834045538

> <JCHEM_PKA_STRONGEST_BASIC>
3.23678041940132

> <JCHEM_POLAR_SURFACE_AREA>
61.39

> <JCHEM_REFRACTIVITY>
73.9764

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.89e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-{2-[(4-chlorophenyl)formamido]ethyl}morpholin-4-ium-4-olate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0257269
     RDKit          3D
Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide
 36 37  0  0  0  0  0  0  0  0999 V2000
   -1.9905   -1.6145   -1.4270 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1886   -0.6289   -0.6596 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0792   -0.0284   -0.0424 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2438   -0.5306   -0.2849 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3006    0.2534    0.4731 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5788   -0.3217    0.1667 N   0  0  0  0  0  4  0  0  0  0  0  0
    2.4629   -1.4575   -0.5737 O   0  0  0  0  0  1  0  0  0  0  0  0
    3.3695   -0.6403    1.3197 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6815    0.1070    1.3603 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4315   -0.0654    0.2051 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6682   -0.0578   -0.9483 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3373    0.6143   -0.6745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5644   -0.1610   -0.4511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8566    0.8925    0.3596 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1634    1.3369    0.5575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1654    0.6707   -0.0995 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8360    1.1567    0.0876 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -5.9044   -0.3957   -0.9243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6073   -0.7937   -1.0862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2091    0.7772    0.5887 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4284   -0.5062   -1.3708 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3414   -1.5962    0.0420 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0656    0.2490    1.5457 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2437    1.3042    0.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5695   -1.7460    1.4053 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8140   -0.3608    2.2413 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4819    1.1580    1.5818 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2795   -0.3185    2.1964 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4444   -1.1166   -1.2037 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1745    0.4386   -1.7989 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5035    1.5773   -0.1588 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7561    0.7503   -1.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0969    1.4428    0.8940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3778    2.1861    1.2136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7061   -0.9320   -1.4527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4309   -1.6436   -1.7475 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
  2 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 12  6  1  0
 19 13  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  8 25  1  0
  8 26  1  0
  9 27  1  0
  9 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
 12 32  1  0
 14 33  1  0
 15 34  1  0
 18 35  1  0
 19 36  1  0
M  CHG  2   6   1   7  -1
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0      -1.539  -4.674   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.355  -3.368   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.632  -2.008   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -0.093  -1.954   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.723  -3.260   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       0.000  -4.620   0.000  0.00  0.00           N+1
HETATM    7  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       4.001  -5.390   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   18 Cl   UNK     0      10.669  -7.700   0.000  0.00  0.00          Cl+0
HETATM   19  O   UNK     0       0.107  -6.156   0.000  0.00  0.00           O-1
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1    7   19                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18   15                                                            
CONECT   19    6                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   40    0
END

COMPND    HMDB0257269
HETATM    1  O1  UNL     1      -1.991  -1.615  -1.427  1.00  0.00           O  
HETATM    2  C1  UNL     1      -2.189  -0.629  -0.660  1.00  0.00           C  
HETATM    3  N1  UNL     1      -1.079  -0.028  -0.042  1.00  0.00           N  
HETATM    4  C2  UNL     1       0.244  -0.531  -0.285  1.00  0.00           C  
HETATM    5  C3  UNL     1       1.301   0.253   0.473  1.00  0.00           C  
HETATM    6  N2  UNL     1       2.579  -0.322   0.167  1.00  0.00           N1+
HETATM    7  O2  UNL     1       2.463  -1.457  -0.574  1.00  0.00           O1-
HETATM    8  C4  UNL     1       3.369  -0.640   1.320  1.00  0.00           C  
HETATM    9  C5  UNL     1       4.682   0.107   1.360  1.00  0.00           C  
HETATM   10  O3  UNL     1       5.431  -0.065   0.205  1.00  0.00           O  
HETATM   11  C6  UNL     1       4.668  -0.058  -0.948  1.00  0.00           C  
HETATM   12  C7  UNL     1       3.337   0.614  -0.675  1.00  0.00           C  
HETATM   13  C8  UNL     1      -3.564  -0.161  -0.451  1.00  0.00           C  
HETATM   14  C9  UNL     1      -3.857   0.892   0.360  1.00  0.00           C  
HETATM   15  C10 UNL     1      -5.163   1.337   0.558  1.00  0.00           C  
HETATM   16  C11 UNL     1      -6.165   0.671  -0.099  1.00  0.00           C  
HETATM   17 CL1  UNL     1      -7.836   1.157   0.088  1.00  0.00          CL  
HETATM   18  C12 UNL     1      -5.904  -0.396  -0.924  1.00  0.00           C  
HETATM   19  C13 UNL     1      -4.607  -0.794  -1.086  1.00  0.00           C  
HETATM   20  H1  UNL     1      -1.209   0.777   0.589  1.00  0.00           H  
HETATM   21  H2  UNL     1       0.428  -0.506  -1.371  1.00  0.00           H  
HETATM   22  H3  UNL     1       0.341  -1.596   0.042  1.00  0.00           H  
HETATM   23  H4  UNL     1       1.066   0.249   1.546  1.00  0.00           H  
HETATM   24  H5  UNL     1       1.244   1.304   0.082  1.00  0.00           H  
HETATM   25  H6  UNL     1       3.570  -1.746   1.405  1.00  0.00           H  
HETATM   26  H7  UNL     1       2.814  -0.361   2.241  1.00  0.00           H  
HETATM   27  H8  UNL     1       4.482   1.158   1.582  1.00  0.00           H  
HETATM   28  H9  UNL     1       5.280  -0.319   2.196  1.00  0.00           H  
HETATM   29  H10 UNL     1       4.444  -1.117  -1.204  1.00  0.00           H  
HETATM   30  H11 UNL     1       5.174   0.439  -1.799  1.00  0.00           H  
HETATM   31  H12 UNL     1       3.503   1.577  -0.159  1.00  0.00           H  
HETATM   32  H13 UNL     1       2.756   0.750  -1.599  1.00  0.00           H  
HETATM   33  H14 UNL     1      -3.097   1.443   0.894  1.00  0.00           H  
HETATM   34  H15 UNL     1      -5.378   2.186   1.214  1.00  0.00           H  
HETATM   35  H16 UNL     1      -6.706  -0.932  -1.453  1.00  0.00           H  
HETATM   36  H17 UNL     1      -4.431  -1.644  -1.748  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   13
CONECT    3    4   20
CONECT    4    5   21   22
CONECT    5    6   23   24
CONECT    6    7    8   12
CONECT    8    9   25   26
CONECT    9   10   27   28
CONECT   10   11
CONECT   11   12   29   30
CONECT   12   31   32
CONECT   13   14   14   19
CONECT   14   15   33
CONECT   15   16   16   34
CONECT   16   17   18
CONECT   18   19   19   35
CONECT   19   36
END

HMDB0257269
     RDKit          3D
Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide
 36 37  0  0  0  0  0  0  0  0999 V2000
   -1.9905   -1.6145   -1.4270 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1886   -0.6289   -0.6596 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0792   -0.0284   -0.0424 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2438   -0.5306   -0.2849 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3006    0.2534    0.4731 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5788   -0.3217    0.1667 N   0  0  0  0  0  4  0  0  0  0  0  0
    2.4629   -1.4575   -0.5737 O   0  0  0  0  0  1  0  0  0  0  0  0
    3.3695   -0.6403    1.3197 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6815    0.1070    1.3603 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4315   -0.0654    0.2051 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6682   -0.0578   -0.9483 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3373    0.6143   -0.6745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5644   -0.1610   -0.4511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8566    0.8925    0.3596 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1634    1.3369    0.5575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1654    0.6707   -0.0995 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8360    1.1567    0.0876 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -5.9044   -0.3957   -0.9243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6073   -0.7937   -1.0862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2091    0.7772    0.5887 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4284   -0.5062   -1.3708 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3414   -1.5962    0.0420 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0656    0.2490    1.5457 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2437    1.3042    0.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5695   -1.7460    1.4053 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8140   -0.3608    2.2413 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4819    1.1580    1.5818 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2795   -0.3185    2.1964 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4444   -1.1166   -1.2037 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1745    0.4386   -1.7989 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5035    1.5773   -0.1588 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7561    0.7503   -1.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0969    1.4428    0.8940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3778    2.1861    1.2136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7061   -0.9320   -1.4527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4309   -1.6436   -1.7475 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
  2 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 12  6  1  0
 19 13  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  8 25  1  0
  8 26  1  0
  9 27  1  0
  9 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
 12 32  1  0
 14 33  1  0
 15 34  1  0
 18 35  1  0
 19 36  1  0
M  CHG  2   6   1   7  -1
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₃H₁₇ClN₂O₃

Average Molecular Weight

284.74

Monoisotopic Molecular Weight

284.0927701

IUPAC Name

4-{2-[(4-chlorophenyl)formamido]ethyl}morpholin-4-ium-4-olate

Traditional Name

4-{2-[(4-chlorophenyl)formamido]ethyl}morpholin-4-ium-4-olate

CAS Registry Number

Not Available

SMILES

[O-][N+]1(CCNC(=O)C2=CC=C(Cl)C=C2)CCOCC1

InChI Identifier

InChI=1S/C13H17ClN2O3/c14-12-3-1-11(2-4-12)13(17)15-5-6-16(18)7-9-19-10-8-16/h1-4H,5-10H2,(H,15,17)

InChI Key

CJTZZADPEGGIMM-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 4-halobenzoic acids and derivatives. These are benzoic acids or derivatives carrying a halogen atom at the 4-position of the benzene ring.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

4-halobenzoic acids and derivatives

Alternative Parents

Substituents

4-halobenzoic acid or derivatives
Benzamide
Benzoyl
Halobenzene
Chlorobenzene
Oxazinane
Morpholine
Aryl halide
Aryl chloride
Trialkyl amine oxide
Secondary carboxylic acid amide
Carboxamide group
Oxacycle
Azacycle
Organoheterocyclic compound
Trisubstituted n-oxide
Ether
Dialkyl ether
Carboxylic acid derivative
N-oxide
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organic zwitterion
Organooxygen compound
Organonitrogen compound
Organochloride
Organohalogen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

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	0.38	ALOGPS
logP	0.33	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	14.66	ChemAxon
pKa (Strongest Basic)	3.24	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	61.39 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	73.98 m³·mol⁻¹	ChemAxon
Polarizability	29.11 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]+	156.111	30932474
DeepCCS	[M-H]-	153.716	30932474
DeepCCS	[M-2H]-	186.827	30932474
DeepCCS	[M+Na]+	162.024	30932474
AllCCS	[M+H]+	162.4	32859911
AllCCS	[M+H-H2O]+	158.9	32859911
AllCCS	[M+NH4]+	165.7	32859911
AllCCS	[M+Na]+	166.6	32859911
AllCCS	[M-H]-	165.2	32859911
AllCCS	[M+Na-2H]-	165.4	32859911
AllCCS	[M+HCOO]-	165.8	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide	[O-][N+]1(CCNC(=O)C2=CC=C(Cl)C=C2)CCOCC1	3258.0	Standard polar	33892256
Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide	[O-][N+]1(CCNC(=O)C2=CC=C(Cl)C=C2)CCOCC1	1874.0	Standard non polar	33892256
Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide	[O-][N+]1(CCNC(=O)C2=CC=C(Cl)C=C2)CCOCC1	2380.0	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide,1TMS,isomer #1	C[Si](C)(C)N(CC[N+]1([O-])CCOCC1)C(=O)C1=CC=C(Cl)C=C1	2411.2	Semi standard non polar	33892256
Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide,1TMS,isomer #1	C[Si](C)(C)N(CC[N+]1([O-])CCOCC1)C(=O)C1=CC=C(Cl)C=C1	2247.0	Standard non polar	33892256
Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide,1TMS,isomer #1	C[Si](C)(C)N(CC[N+]1([O-])CCOCC1)C(=O)C1=CC=C(Cl)C=C1	3249.4	Standard polar	33892256
Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N(CC[N+]1([O-])CCOCC1)C(=O)C1=CC=C(Cl)C=C1	2683.1	Semi standard non polar	33892256
Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N(CC[N+]1([O-])CCOCC1)C(=O)C1=CC=C(Cl)C=C1	2484.8	Standard non polar	33892256
Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N(CC[N+]1([O-])CCOCC1)C(=O)C1=CC=C(Cl)C=C1	3330.3	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide GC-MS (Non-derivatized) - 70eV, Positive	splash10-000i-3910000000-000b38a00e719101c279	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide GC-MS (Non-derivatized) - 70eV, Positive	Not Available	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

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

143126

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

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 Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide (HMDB0257269)

MOL for HMDB0257269 (Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide)

3D MOL for HMDB0257269 (Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide)

3D SDF for HMDB0257269 (Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide)

3D-SDF for HMDB0257269 (Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide)

PDB for HMDB0257269 (Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide)

3D PDB for HMDB0257269 (Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide)

SMILES for HMDB0257269 (Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide)

INCHI for HMDB0257269 (Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide)

Structure for HMDB0257269 (Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide)

3D Structure for HMDB0257269 (Benzamide, 4-chloro-N-(2-(4-morpholinyl)ethyl)-, N-oxide)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra