U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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 METHYLHYDROQUINONE

SMILES

CC1=CC(O)=CC=C1O

InChI

InChIKey=CNHDIAIOKMXOLK-UHFFFAOYSA-N
InChI=1S/C7H8O2/c1-5-4-6(8)2-3-7(5)9/h2-4,8-9H,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
Genopalâ„¢: a novel hollow fibre array for focused microarray analysis.
2010-12
Theoretical study on the thermodynamic properties and self-decomposition of methylbenzenediol isomers.
2010-11-04
Gentisides C-K: nine new neuritogenic compounds from the traditional Chinese medicine Gentiana rigescens Franch.
2010-10-01
The redox-sensing regulator YodB senses quinones and diamide via a thiol-disulfide switch in Bacillus subtilis.
2010-09
Biosynthesis and toxicological effects of patulin.
2010-04
Gentisides A and B, two new neuritogenic compounds from the traditional Chinese medicine Gentiana rigescens Franch.
2010-03-15
Genotoxic and Cytotoxic Safety Evaluation of Papain (Carica papaya L.) Using In Vitro Assays.
2010
Synthesis, characterization and texture observations of calamitic liquid crystalline compounds.
2009-11-04
Differences in defensive volatiles of the forked fungus beetle, Bolitotherus cornutus, living on two species of fungus.
2009-11
Transcriptome and proteome analyses of adaptive responses to methyl methanesulfonate in Escherichia coli K-12 and ada mutant strains.
2009-09-03
[Decolorization of azo dyes using quinone reductase and quinoid compounds].
2009-06-15
Acceleration of azo dye decolorization by using quinone reductase activity of azoreductase and quinone redox mediator.
2009-06
Molecular cloning and functional characterization of two CYP619 cytochrome P450s involved in biosynthesis of patulin in Aspergillus clavatus.
2009-05
Electrochemical incineration of cresols: a comparative study between PbO2 and boron-doped diamond anodes.
2009-03
Complementary cooperation between two syntrophic bacteria in pesticide degradation.
2009-02-21
Simple ortho- and para-hydroquinones as compounds neuroprotective against oxidative stress in a manner associated with specific transcriptional activation.
2009-02-06
Regulation of quinone detoxification by the thiol stress sensing DUF24/MarR-like repressor, YodB in Bacillus subtilis.
2008-03
Proteomic signatures uncover thiol-specific electrophile resistance mechanisms in Bacillus subtilis.
2008-02
2,5-dihydroxybenzyl and (1,4-dihydroxy-2-naphthyl)methyl, novel reductively armed photocages for the hydroxyl moiety.
2007-11-23
The MarR-type repressor MhqR (YkvE) regulates multiple dioxygenases/glyoxalases and an azoreductase which confer resistance to 2-methylhydroquinone and catechol in Bacillus subtilis.
2007-10
Transcriptome and proteome analyses in response to 2-methylhydroquinone and 6-brom-2-vinyl-chroman-4-on reveal different degradation systems involved in the catabolism of aromatic compounds in Bacillus subtilis.
2007-05
Pharmacologically active natural products in the defence secretion of Palembus ocularis (Tenebrionidae, Coleoptera).
2006-06-15
Isolation of fenitrothion-degrading strain Burkholderia sp. FDS-1 and cloning of mpd gene.
2006-06
p-hydroxylation reactions catalyzed by naphthalene dioxygenase.
2006-02
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
Characterization of methylhydroquinone-metabolizing oxygenase genes encoded on plasmid in Burkholderia sp. NF100.
2005-11
Nitric oxide promotes strong cytotoxicity of phenolic compounds against Escherichia coli: the influence of antioxidant defenses.
2003-12-01
Oxidative DNA damage induced by toluene is involved in its male reproductive toxicity.
2003-01
Vibrational analysis of substituted phenols: part I. Vibrational spectra, normal coordinate analysis and transferability of force constants of some formyl-, methoxy-, formylmethoxy-, methyl- and halogeno-phenols.
2002-12
Characterization of manganese-dependent peroxidase isoenzymes from the ligninolytic fungus Phanerochaete flavido-alba.
2002-10
Anti-HSV-1 activity of synthetic humic acid-like polymers derived from p-diphenolic starting compounds.
2002-07
Volatile components in dorsal gland secretions of the white-lipped peccary, Tayassu pecari, from Bolivia.
2001-12
Studies of all-trans-retinal as a photooxidizing agent.
2001-01
Selective inhibitory activity of polyhydroxycarboxylates derived from phenolic compounds against human immunodeficiency virus replication.
1991
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:34:29 GMT 2025
Edited
by admin
on Mon Mar 31 19:34:29 GMT 2025
Record UNII
332W51E0OC
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-4962
Preferred Name English
METHYLHYDROQUINONE
Systematic Name English
2-METHYLHYDROQUINONE
Systematic Name English
2-METHYL-1,4-BENZENEDIOL
Systematic Name English
TOLYLHYDROQUINONE
Systematic Name English
P-TOLUHYDROQUINOL
Common Name English
Code System Code Type Description
CAS
95-71-6
Created by admin on Mon Mar 31 19:34:29 GMT 2025 , Edited by admin on Mon Mar 31 19:34:29 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-443-7
Created by admin on Mon Mar 31 19:34:29 GMT 2025 , Edited by admin on Mon Mar 31 19:34:29 GMT 2025
PRIMARY
PUBCHEM
7253
Created by admin on Mon Mar 31 19:34:29 GMT 2025 , Edited by admin on Mon Mar 31 19:34:29 GMT 2025
PRIMARY
FDA UNII
332W51E0OC
Created by admin on Mon Mar 31 19:34:29 GMT 2025 , Edited by admin on Mon Mar 31 19:34:29 GMT 2025
PRIMARY
CHEBI
133842
Created by admin on Mon Mar 31 19:34:29 GMT 2025 , Edited by admin on Mon Mar 31 19:34:29 GMT 2025
PRIMARY
EPA CompTox
DTXSID4020876
Created by admin on Mon Mar 31 19:34:29 GMT 2025 , Edited by admin on Mon Mar 31 19:34:29 GMT 2025
PRIMARY
NSC
4962
Created by admin on Mon Mar 31 19:34:29 GMT 2025 , Edited by admin on Mon Mar 31 19:34:29 GMT 2025
PRIMARY
MESH
C062397
Created by admin on Mon Mar 31 19:34:29 GMT 2025 , Edited by admin on Mon Mar 31 19:34:29 GMT 2025
PRIMARY