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Details

Stereochemistry ACHIRAL
Molecular Formula C8H10O
Molecular Weight 122.1644
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,3-DIMETHYLPHENOL

SMILES

CC1=CC=CC(O)=C1C

InChI

InChIKey=QWBBPBRQALCEIZ-UHFFFAOYSA-N
InChI=1S/C8H10O/c1-6-4-3-5-8(9)7(6)2/h3-5,9H,1-2H3

HIDE SMILES / InChI

Molecular Formula C8H10O
Molecular Weight 122.1644
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
4-Bromo-methyl-7,8-dimethyl-coumarin.
2010-11-30
Musculoskeletal response to whole-body vibration during fracture healing in intact and ovariectomized rats.
2010-08
Estrogen and raloxifene improve metaphyseal fracture healing in the early phase of osteoporosis. A new fracture-healing model at the tibia in rat.
2010-02
Three dimensional model for N-terminal A domain of DmpR (2-dimethylphenol) protein based on secondary structure prediction and fold recognition.
2010
Solid-phase microextraction Ni-Ti fibers coated with functionalised silica particles immobilized in a sol-gel matrix.
2009-03-20
Determination of gas-phase acidities of dimethylphenols: combined experimental and theoretical study.
2008-11
Disassembly of lignin and chemical recovery in supercritical water and p-cresol mixture. Studies on lignin model compounds.
2008-04
Immunomodulatory effects of mono-, di-, and trimethylphenols in mice.
2007-03-22
Determination of phenolic compounds in wastewater by liquid-phase microextraction coupled with gas chromatography.
2007-01-27
Twisted, Z-shaped perylene bisimide.
2006-01-25
Glucuronidation converts gemfibrozil to a potent, metabolism-dependent inhibitor of CYP2C8: implications for drug-drug interactions.
2006-01
[Degradation of phenols formed during lignin pyrolysis by microfungi of genera Trichoderma and Penicillium].
2005-10-26
Protein engineering of toluene-o-xylene monooxygenase from Pseudomonas stutzeri OX1 for enhanced chlorinated ethene degradation and o-xylene oxidation.
2005-09
Occupational exposure to aromatic hydrocarbons at a coke plant: Part I. Identification of hydrocarbons in air and their metabolites in urine by a gas chromatography-mass spectrometry method.
2004-05
Synthesis of pyrimidine derivatives possessing an antioxidative property and their inhibitory effects on picryl chloride-induced contact hypersensitivity reaction.
2003-12
Synthesis and SAR studies of potent HIV protease inhibitors containing novel dimethylphenoxyl acetates as P2 ligands.
2003-11-03
Vibrational analysis of substituted phenols: part II. Transferability of valence force constants.
2002-12
Procedure for the quantification of rider peaks.
2001-09-21
Characterization of Rhodococcus opacus R7, a strain able to degrade naphthalene and o-xylene isolated from a polycyclic aromatic hydrocarbon-contaminated soil.
2001-09
Photorelease of HCl from o-methylphenacyl chloride proceeds through the Z-xylylenol.
2001-08-15
Isolation and characterization of a thermotolerant bacterium Ralstonia sp. strain PHS1 that degrades benzene, toluene, ethylbenzene, and o-xylene.
2001-07
Solid-state photochromism and photoreactivity of o- and p-anisaldehydes. Remarkable stabilization of o-xylylenols.
2001-05-17
[Research on a new side-chain liquid crystalline polysiloxane as stationary phase for capillary column gas chromatography].
2001-05
Determination of Henry's law constants of phenols by pervaporation-flow injection analysis.
2001-01-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:21:39 GMT 2025
Edited
by admin
on Mon Mar 31 19:21:39 GMT 2025
Record UNII
RLF9YS3586
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
XYLENOL 2,3-DIMETHYLPHENOL
MI  
Preferred Name English
2,3-DIMETHYLPHENOL
HSDB  
Systematic Name English
METACRESOL IMPURITY I [EP IMPURITY]
Common Name English
2,3-DIMETHYLPHENOL [HSDB]
Common Name English
2,3-XYLENOL
Systematic Name English
NSC-62011
Code English
XYLENOL 2,3-DIMETHYLPHENOL [MI]
Common Name English
DIMETHYLPHENOL, 2,3-
Systematic Name English
Code System Code Type Description
PUBCHEM
10687
Created by admin on Mon Mar 31 19:21:39 GMT 2025 , Edited by admin on Mon Mar 31 19:21:39 GMT 2025
PRIMARY
HSDB
5676
Created by admin on Mon Mar 31 19:21:39 GMT 2025 , Edited by admin on Mon Mar 31 19:21:39 GMT 2025
PRIMARY
FDA UNII
RLF9YS3586
Created by admin on Mon Mar 31 19:21:39 GMT 2025 , Edited by admin on Mon Mar 31 19:21:39 GMT 2025
PRIMARY
MESH
C054067
Created by admin on Mon Mar 31 19:21:39 GMT 2025 , Edited by admin on Mon Mar 31 19:21:39 GMT 2025
PRIMARY
CAS
526-75-0
Created by admin on Mon Mar 31 19:21:39 GMT 2025 , Edited by admin on Mon Mar 31 19:21:39 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-395-3
Created by admin on Mon Mar 31 19:21:39 GMT 2025 , Edited by admin on Mon Mar 31 19:21:39 GMT 2025
PRIMARY
NSC
62011
Created by admin on Mon Mar 31 19:21:39 GMT 2025 , Edited by admin on Mon Mar 31 19:21:39 GMT 2025
PRIMARY
EPA CompTox
DTXSID6025143
Created by admin on Mon Mar 31 19:21:39 GMT 2025 , Edited by admin on Mon Mar 31 19:21:39 GMT 2025
PRIMARY
MERCK INDEX
m11549
Created by admin on Mon Mar 31 19:21:39 GMT 2025 , Edited by admin on Mon Mar 31 19:21:39 GMT 2025
PRIMARY Merck Index
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (GC)
EP