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Details

Stereochemistry ACHIRAL
Molecular Formula C7H6O3
Molecular Weight 138.1207
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,5-DIHYDROXYBENZALDEHYDE

SMILES

OC1=CC=C(O)C(C=O)=C1

InChI

InChIKey=CLFRCXCBWIQVRN-UHFFFAOYSA-N
InChI=1S/C7H6O3/c8-4-5-3-6(9)1-2-7(5)10/h1-4,9-10H

HIDE SMILES / InChI

Molecular Formula C7H6O3
Molecular Weight 138.1207
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Analysis of aliphatic amines in air samples by HPLC with electrochemical detection.
2002 Aug 1
Effects of aldehyde dehydrogenase-2 genetic polymorphisms on metabolism of structurally different aldehydes in human liver.
2002 Jan
Anti-HSV-1 activity of synthetic humic acid-like polymers derived from p-diphenolic starting compounds.
2002 Jul
Simultaneous determination of amphetamine and one of its metabolites by HPLC with electrochemical detection.
2002 Sep 5
Tyrosol degradation via the homogentisic acid pathway in a newly isolated Halomonas strain from olive processing effluents.
2008 Dec
N'-(2,5-Dihydroxy-benzyl-idene)benzene-sulfonohydrazide.
2008 Jan 25
2,5-Dihydroxy-benzaldehyde 4-methyl-thio-semicarbazone.
2008 Jun 28
Photolabile protection of 1,2- and 1,3-diols with salicylaldehyde derivatives.
2008 Nov 20
3-[(E)-2-(5,7-Dichloro-8-hydroxy-quinolin-2-yl)vin-yl]-4-hydroxy-phenyl acetate.
2009 Feb 11
(E)-2-[(2,4-Dichloro-phen-yl)imino-meth-yl]benzene-1,4-diol monohydrate.
2009 Nov 7
2,2'-o-Phenyl-enediacetonitrile.
2009 Oct 17
(E)-2-[3-(Trifluoro-meth-yl)phenyl-imino-meth-yl]benzene-1,4-diol.
2009 Oct 17
Biosynthesis and toxicological effects of patulin.
2010 Apr
N'-(2,5-Dihydroxy-benzyl-idene)-2-hydr-oxy-3-methyl-benzohydrazide.
2010 Apr 17
(E)-4-Hy-droxy-2-[(2-hy-droxy-phen-yl)iminiometh-yl]phenolate.
2010 Jun 5
Liquid chromatographic/electrospray ionization mass spectrometric identification of the oxidation end-products of trans-resveratrol in aqueous solutions.
2010 Mar 15
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:10:15 GMT 2023
Edited
by admin
on Fri Dec 15 19:10:15 GMT 2023
Record UNII
0Q83HDS90W
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,5-DIHYDROXYBENZALDEHYDE
Systematic Name English
FORMYLHYDROQUINONE
Systematic Name English
DIHYDROXYBENZALDEHYDE, 2,5-
Systematic Name English
GENTISALDEHYDE
Systematic Name English
NSC-72387
Code English
BENZALDEHYDE, 2,5-DIHYDROXY-
Systematic Name English
5-HYDROXYSALICYLALDEHYDE
Systematic Name English
Code System Code Type Description
CHEBI
28508
Created by admin on Fri Dec 15 19:10:15 GMT 2023 , Edited by admin on Fri Dec 15 19:10:15 GMT 2023
PRIMARY
FDA UNII
0Q83HDS90W
Created by admin on Fri Dec 15 19:10:15 GMT 2023 , Edited by admin on Fri Dec 15 19:10:15 GMT 2023
PRIMARY
PUBCHEM
70949
Created by admin on Fri Dec 15 19:10:15 GMT 2023 , Edited by admin on Fri Dec 15 19:10:15 GMT 2023
PRIMARY
NSC
72387
Created by admin on Fri Dec 15 19:10:15 GMT 2023 , Edited by admin on Fri Dec 15 19:10:15 GMT 2023
PRIMARY
EPA CompTox
DTXSID1061601
Created by admin on Fri Dec 15 19:10:15 GMT 2023 , Edited by admin on Fri Dec 15 19:10:15 GMT 2023
PRIMARY
ECHA (EC/EINECS)
214-789-6
Created by admin on Fri Dec 15 19:10:15 GMT 2023 , Edited by admin on Fri Dec 15 19:10:15 GMT 2023
PRIMARY
CAS
1194-98-5
Created by admin on Fri Dec 15 19:10:15 GMT 2023 , Edited by admin on Fri Dec 15 19:10:15 GMT 2023
PRIMARY