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Details

Stereochemistry ACHIRAL
Molecular Formula C8H10O3
Molecular Weight 154.1632
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,3-DIMETHOXYPHENOL

SMILES

COC1=C(OC)C(O)=CC=C1

InChI

InChIKey=QSZCGGBDNYTQHH-UHFFFAOYSA-N
InChI=1S/C8H10O3/c1-10-7-5-3-4-6(9)8(7)11-2/h3-5,9H,1-2H3

HIDE SMILES / InChI

Molecular Formula C8H10O3
Molecular Weight 154.1632
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
(E)-1-(2-Hy-droxy-4,6-dimeth-oxy-phen-yl)-3-(4-meth-oxy-phen-yl)prop-2-en-1-one from Kaempferia rotunda Val.
2010-10-30
Flavokavain B from the rhizome of Alpinia mutica Roxb.
2010-10-20
Fungal laccases: production, function, and applications in food processing.
2010-09-21
Parallel metatranscriptome analyses of host and symbiont gene expression in the gut of the termite Reticulitermes flavipes.
2009-10-15
Synthesis and cosmetic whitening effect of glycosides derived from several phenylpropanoids.
2006-03
Synthesis of pyrimidine derivatives possessing an antioxidative property and their inhibitory effects on picryl chloride-induced contact hypersensitivity reaction.
2003-12
Purification and characterisation of a novel laccase from the ascomycete Melanocarpus albomyces.
2002-07
Dimethoxyphenol oxidase activity of different microbial blue multicopper proteins.
2001-10-16
Characterization of a novel laccase produced by the wood-rotting fungus Phellinus ribis.
2001-08-15
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:37:51 GMT 2025
Edited
by admin
on Mon Mar 31 19:37:51 GMT 2025
Record UNII
OW147I6C84
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,3-DIMETHOXYPHENOL
Systematic Name English
NSC-80659
Preferred Name English
1-HYDROXY-2,3-DIMETHOXYBENZENE
Systematic Name English
PHENOL, 2,3-DIMETHOXY-
Systematic Name English
DIMETHOXY-PHENOL
Systematic Name English
Code System Code Type Description
CAS
5150-42-5
Created by admin on Mon Mar 31 19:37:51 GMT 2025 , Edited by admin on Mon Mar 31 19:37:51 GMT 2025
PRIMARY
NSC
80659
Created by admin on Mon Mar 31 19:37:51 GMT 2025 , Edited by admin on Mon Mar 31 19:37:51 GMT 2025
PRIMARY
PUBCHEM
78828
Created by admin on Mon Mar 31 19:37:51 GMT 2025 , Edited by admin on Mon Mar 31 19:37:51 GMT 2025
PRIMARY
ECHA (EC/EINECS)
225-922-2
Created by admin on Mon Mar 31 19:37:51 GMT 2025 , Edited by admin on Mon Mar 31 19:37:51 GMT 2025
PRIMARY
FDA UNII
OW147I6C84
Created by admin on Mon Mar 31 19:37:51 GMT 2025 , Edited by admin on Mon Mar 31 19:37:51 GMT 2025
PRIMARY