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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2013-05-17 00:50:47 UTC
Update Date2023-02-21 17:29:51 UTC
HMDB IDHMDB0060303
Secondary Accession Numbers
  • HMDB60303
Metabolite Identification
Common Name(2-Naphthyl)methanol
Description(2-Naphthyl)methanol belongs to the class of organic compounds known as naphthalenes. Naphthalenes are compounds containing a naphthalene moiety, which consists of two fused benzene rings (2-Naphthyl)methanol is an extremely weak basic (essentially neutral) compound (based on its pKa) (2-Naphthyl)methanol exists in all living organisms, ranging from bacteria to humans. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings.
Structure
Data?1677000591
Synonyms
ValueSource
2-HydroxymethylnaphthaleneChEBI
2-NaphthalenemethanolChEBI
Naphthalen-2-yl-methanolChEBI
Chemical FormulaC11H10O
Average Molecular Weight158.1965
Monoisotopic Molecular Weight158.073164942
IUPAC Namenaphthalen-2-ylmethanol
Traditional Name2-naphthalenemethanol
CAS Registry NumberNot Available
SMILES
OCC1=CC2=CC=CC=C2C=C1
InChI Identifier
InChI=1S/C11H10O/c12-8-9-5-6-10-3-1-2-4-11(10)7-9/h1-7,12H,8H2
InChI KeyMFGWMAAZYZSWMY-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as naphthalenes. Naphthalenes are compounds containing a naphthalene moiety, which consists of two fused benzene rings.
KingdomOrganic compounds
Super ClassBenzenoids
ClassNaphthalenes
Sub ClassNot Available
Direct ParentNaphthalenes
Alternative Parents
Substituents
  • Naphthalene
  • Organic oxygen compound
  • Hydrocarbon derivative
  • Aromatic alcohol
  • Primary alcohol
  • Organooxygen compound
  • Alcohol
  • Aromatic homopolycyclic compound
Molecular FrameworkAromatic homopolycyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.29 g/LALOGPS
logP2.28ALOGPS
logP2.2ChemAxon
logS-2.7ALOGPS
pKa (Strongest Acidic)14.96ChemAxon
pKa (Strongest Basic)-2.8ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area20.23 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity49.32 m³·mol⁻¹ChemAxon
Polarizability17.75 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+134.30331661259
DarkChem[M-H]-132.33231661259
DeepCCS[M+H]+133.65330932474
DeepCCS[M-H]-130.26630932474
DeepCCS[M-2H]-167.38130932474
DeepCCS[M+Na]+142.9230932474
AllCCS[M+H]+133.132859911
AllCCS[M+H-H2O]+128.432859911
AllCCS[M+NH4]+137.432859911
AllCCS[M+Na]+138.732859911
AllCCS[M-H]-134.432859911
AllCCS[M+Na-2H]-135.032859911
AllCCS[M+HCOO]-135.732859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
(2-Naphthyl)methanolOCC1=CC2=CC=CC=C2C=C12707.0Standard polar33892256
(2-Naphthyl)methanolOCC1=CC2=CC=CC=C2C=C11508.9Standard non polar33892256
(2-Naphthyl)methanolOCC1=CC2=CC=CC=C2C=C11572.4Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
(2-Naphthyl)methanol,1TMS,isomer #1C[Si](C)(C)OCC1=CC=C2C=CC=CC2=C11644.4Semi standard non polar33892256
(2-Naphthyl)methanol,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC1=CC=C2C=CC=CC2=C11887.9Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - (2-Naphthyl)methanol GC-MS (Non-derivatized) - 70eV, Positivesplash10-0006-0900000000-a1ebc0a2f19b9c0d4e7e2017-09-20Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (2-Naphthyl)methanol GC-MS (1 TMS) - 70eV, Positivesplash10-00dl-9840000000-7fa39974238f6920c1412017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (2-Naphthyl)methanol GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2-Naphthyl)methanol 10V, Positive-QTOFsplash10-0a4l-0900000000-6ab588a370ce42b901022015-09-14Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2-Naphthyl)methanol 20V, Positive-QTOFsplash10-0006-0900000000-4315070c5866b93000972015-09-14Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2-Naphthyl)methanol 40V, Positive-QTOFsplash10-0006-1900000000-bfc5712522445e2222342015-09-14Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2-Naphthyl)methanol 10V, Negative-QTOFsplash10-0a4i-0900000000-76b234c378af36dccd112015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2-Naphthyl)methanol 20V, Negative-QTOFsplash10-0a6r-0900000000-328e6b0c35f9a435784e2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2-Naphthyl)methanol 40V, Negative-QTOFsplash10-004i-0900000000-56f0eb46d9782efaee972015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2-Naphthyl)methanol 10V, Positive-QTOFsplash10-0006-0900000000-cf41caaf3a69a30066d72021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2-Naphthyl)methanol 20V, Positive-QTOFsplash10-0006-0900000000-b61c0dc3bc60b1b44ed42021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2-Naphthyl)methanol 40V, Positive-QTOFsplash10-002f-1900000000-c263fa3ba2ca364234d52021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2-Naphthyl)methanol 10V, Negative-QTOFsplash10-004i-0900000000-ec6816397577a7beb93f2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2-Naphthyl)methanol 20V, Negative-QTOFsplash10-004i-0900000000-ec6816397577a7beb93f2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (2-Naphthyl)methanol 40V, Negative-QTOFsplash10-004i-0900000000-44d15af39bc9b047880b2021-10-12Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, H2O, predicted)2022-08-18Wishart LabView Spectrum

IR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M-H]-)2023-02-04FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)2023-02-04FELIX labView Spectrum
Biological Properties
Cellular Locations
  • Membrane (predicted from logP)
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDC02909
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound74128
PDB IDNot Available
ChEBI ID27615
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Magrane M: UniProt Knowledgebase: a hub of integrated protein data. Database (Oxford). 2011 Mar 29;2011:bar009. doi: 10.1093/database/bar009. Print 2011. [PubMed:21447597 ]

Enzymes

General function:
Involved in zinc ion binding
Specific function:
Class-III ADH is remarkably ineffective in oxidizing ethanol, but it readily catalyzes the oxidation of long-chain primary alcohols and the oxidation of S-(hydroxymethyl) glutathione.
Gene Name:
ADH5
Uniprot ID:
P11766
Molecular weight:
39723.945
Reactions
(2-Naphthyl)methanol + NAD → 2-Naphthaldehyde + NADH + Hydrogen Iondetails