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Details

Stereochemistry ACHIRAL
Molecular Formula C7H8O2
Molecular Weight 124.1372
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of M-HYDROXYANISOLE

SMILES

COC1=CC=CC(O)=C1

InChI

InChIKey=ASHGTJPOSUFTGB-UHFFFAOYSA-N
InChI=1S/C7H8O2/c1-9-7-4-2-3-6(8)5-7/h2-5,8H,1H3

HIDE SMILES / InChI

Molecular Formula C7H8O2
Molecular Weight 124.1372
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Pairwise substitution effects, inter- and intramolecular hydrogen bonds in methoxyphenols and dimethoxybenzenes. Thermochemistry, calorimetry, and first-principles calculations.
2010-12-16
Benzyl N-[(S)-2-hy-droxy-1-({[(E)-2-hy-droxy-4-meth-oxy-benzyl-idene]hydrazin-yl}carbon-yl)eth-yl]carbamate.
2010-11-20
Rate coefficients for the gas-phase reaction of hydroxyl radicals with 2-methoxyphenol (guaiacol) and related compounds.
2010-11-04
Structure-toxicity relationship of phenolic analogs as anti-melanoma agents: an enzyme directed prodrug approach.
2010-02-12
(E)-2-[(4-Fluoro-phen-yl)imino-meth-yl]-5-methoxy-phenol.
2010-01-09
The bromination kinetics of phenolic compounds in aqueous solution.
2009-10-30
Antioxidant hydroquinones substituted by beta-1,6-linked oligosaccharides in wheat germ.
2009-04
4-(3-Methoxy-phen-oxy)butyric acid.
2009-03-19
Thermochemistry and gas-phase ion energetics of 2-hydroxy-4-methoxy-benzophenone (oxybenzone).
2008-04-10
A meta effect in nonphotochemical processes: the homolytic chemistry of m-methoxyphenol.
2008-03-21
Study of some UV filters stability in chlorinated water and identification of halogenated by-products by gas chromatography-mass spectrometry.
2008-01-18
An efficient and scalable synthesis of substituted phenanthrenequinones by intramolecular Friedel-Crafts reaction of imidazolides.
2007-10-11
Changes in key odorants of raw coffee beans during storage under defined conditions.
2007-07-11
Alanine 101 and alanine 110 of the alpha subunit of Pseudomonas stutzeri OX1 toluene-o-xylene monooxygenase influence the regiospecific oxidation of aromatics.
2005-12-05
Effect of phenolic mediators and humic acid on cyprodinil transformation in presence of birnessite.
2004-06
Total synthesis of 10-norparvulenone and of O-methylasparvenone using a xanthate-mediated free radical addition-cyclization sequence.
2003-10-02
Metabolic activation of 3-hydroxyanisole by isolated rat hepatocytes.
2003-01-06
Isolation and characterization of a veratrol:corrinoid protein methyl transferase from Acetobacterium dehalogenans.
2001-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:17:34 GMT 2025
Edited
by admin
on Mon Mar 31 19:17:34 GMT 2025
Record UNII
HXB7441U87
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ORISTAR HOA
Preferred Name English
M-HYDROXYANISOLE
INCI  
INCI  
Official Name English
3-HYDROXYANISOLE
Systematic Name English
PHENOL, M-METHOXY-
Systematic Name English
M-METHOXYPHENOL
Systematic Name English
PHENOL, 3-METHOXY-
Systematic Name English
NSC-21735
Code English
3-METHOXYPHENOL
Systematic Name English
RESORCINOL METHYL ETHER
Systematic Name English
1-HYDROXY-3-METHOXYBENZENE
Systematic Name English
M-GUAIACOL
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
205-754-6
Created by admin on Mon Mar 31 19:17:34 GMT 2025 , Edited by admin on Mon Mar 31 19:17:34 GMT 2025
PRIMARY
EPA CompTox
DTXSID0022012
Created by admin on Mon Mar 31 19:17:34 GMT 2025 , Edited by admin on Mon Mar 31 19:17:34 GMT 2025
PRIMARY
CAS
150-19-6
Created by admin on Mon Mar 31 19:17:34 GMT 2025 , Edited by admin on Mon Mar 31 19:17:34 GMT 2025
PRIMARY
NSC
21735
Created by admin on Mon Mar 31 19:17:34 GMT 2025 , Edited by admin on Mon Mar 31 19:17:34 GMT 2025
PRIMARY
CHEBI
52678
Created by admin on Mon Mar 31 19:17:34 GMT 2025 , Edited by admin on Mon Mar 31 19:17:34 GMT 2025
PRIMARY
MESH
C094702
Created by admin on Mon Mar 31 19:17:34 GMT 2025 , Edited by admin on Mon Mar 31 19:17:34 GMT 2025
PRIMARY
PUBCHEM
9007
Created by admin on Mon Mar 31 19:17:34 GMT 2025 , Edited by admin on Mon Mar 31 19:17:34 GMT 2025
PRIMARY
FDA UNII
HXB7441U87
Created by admin on Mon Mar 31 19:17:34 GMT 2025 , Edited by admin on Mon Mar 31 19:17:34 GMT 2025
PRIMARY