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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 2,4-DIHYDROXYBENZALDEHYDE

SMILES

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

InChI

InChIKey=IUNJCFABHJZSKB-UHFFFAOYSA-N
InChI=1S/C7H6O3/c8-4-5-1-2-6(9)3-7(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
2-[(2,4-Dihydroxy-benzyl-idene)amino]-3',6'-bis-(ethyl-amino)spiro-[isoindoline-1,9'-xanthen]-3-one.
2010-05-29
Bis(μ-5-hydr-oxy-2-{[2-(N-phenyl-thio-carbamo-yl)hydrazin-1-yl-idene]meth-yl}phenolato)bis[chloridozinc(II)] N,N-dimethyl-formamide tetra-solvate.
2010-04-24
4-[(2,4-Dihydroxy-benzyl-idene)ammonio]benzene-sulfonate trihydrate.
2010-02-10
[5,5'-Dihydr-oxy-2,2'-[o-phenyl-enebis(nitrilo-methyl-idyne)]diphenolato}copper(II) methanol disolvate.
2009-12-19
A new Schiff base nickel(II) complex: {5,5'-dihydr-oxy-2,2'-[o-phenyl-enebis(nitrilo-methyl-idyne)]diphenolato}nickel(II) methanol disolvate.
2009-10-13
(E)-2,4-Dihydroxy-benzaldehyde 4-ethyl-thio-semicarbazone-4,4'-bipyridine-water (4/7/2).
2009-08-12
Bis(acetone 4-phenyl-thio-semi-carbazonato-κN,S)zinc(II).
2009-07-22
[1-(4-Hydr-oxy-2-oxidobenzyl-idene)-4-phenyl-thio-semicarbazonato-κN,O,S](1,10-phenanthroline-κN,N')zinc(II)-4,4'-bipyridine (2/1).
2009-07-15
(E)-2-(2,4-Dihydroxy-benzyl-ideneamino)benzonitrile.
2009-06-06
Enantioselective total synthesis of all of the known chiral cleroindicins (C-F): clarification among optical rotations and assignments.
2009-06-05
Bis(μ-4-hydr-oxy-2-oxidobenzaldehyde 4-ethyl-thio-semicarbazone)-κO,N,S:O;κO:O,N,S-bis-[chloridozinc(II)] dimethyl sulfoxide tris-olvate.
2009-04-22
Volatile compounds in acacia, chestnut, cherry, ash, and oak woods, with a view to their use in cooperage.
2009-04-22
2,4-Dihydroxy-benzaldehyde 4-methyl-thio-semicarbazone.
2008-10-31
2,4-Dihydroxy-benzaldehyde 4-ethyl-thio-semicarbazone.
2008-10-18
(Z)-6-{2-[(E)-2,4-Dihydroxy-benzyl-ideneamino]phenyl-amino-methyl-ene}-3-hydroxy-cyclo-hexa-2,4-dienone toluene solvate.
2008-08-20
2-((E)-{2-[(1E)-(2,4-Dihydroxy-benzyl-idene)amino]phen-yl}iminiometh-yl)-5-hydroxy-phenolate methanol solvate.
2008-06-13
3,4-Dihydroxy-benzaldehyde thio-semi-carbazone.
2008-05-14
Low-energy collision-induced fragmentation of negative ions derived from ortho-, meta-, and para-hydroxyphenyl carbaldehydes, ketones, and related compounds.
2007-09
The first total synthesis of kwakhurin, a characteristic component of a rejuvenating plant, "kwao keur": toward an efficient synthetic route to phytoestrogenic isoflavones.
2005-02-21
2,4-Dinitrophenylhydrazones of 2,4-dihydroxybenzaldehyde, 2,4-dihydroxyacetophenone and 2,4-dihydroxybenzophenone.
2004-02
Antibacterial activities of phenolic benzaldehydes and benzoic acids against Campylobacter jejuni, Escherichia coli, Listeria monocytogenes, and Salmonella enterica.
2003-10
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:24:57 GMT 2025
Edited
by admin
on Mon Mar 31 19:24:57 GMT 2025
Record UNII
772JOF6LZS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
.BETA.-RESORCYLALDEHYDE
MI  
Preferred Name English
2,4-DIHYDROXYBENZALDEHYDE
Systematic Name English
.BETA.-RESORCYLALDEHYDE [MI]
Common Name English
DIHYDROXYBENZALDEHYDE, 2,4-
Systematic Name English
2,4-DIHYDROXYBENZENECARBONAL
Common Name English
NSC-8690
Code English
Code System Code Type Description
MERCK INDEX
m9547
Created by admin on Mon Mar 31 19:24:57 GMT 2025 , Edited by admin on Mon Mar 31 19:24:57 GMT 2025
PRIMARY Merck Index
CAS
95-01-2
Created by admin on Mon Mar 31 19:24:57 GMT 2025 , Edited by admin on Mon Mar 31 19:24:57 GMT 2025
PRIMARY
EPA CompTox
DTXSID8021806
Created by admin on Mon Mar 31 19:24:57 GMT 2025 , Edited by admin on Mon Mar 31 19:24:57 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-383-1
Created by admin on Mon Mar 31 19:24:57 GMT 2025 , Edited by admin on Mon Mar 31 19:24:57 GMT 2025
PRIMARY
CHEBI
50198
Created by admin on Mon Mar 31 19:24:57 GMT 2025 , Edited by admin on Mon Mar 31 19:24:57 GMT 2025
PRIMARY
NSC
8690
Created by admin on Mon Mar 31 19:24:57 GMT 2025 , Edited by admin on Mon Mar 31 19:24:57 GMT 2025
PRIMARY
PUBCHEM
7213
Created by admin on Mon Mar 31 19:24:57 GMT 2025 , Edited by admin on Mon Mar 31 19:24:57 GMT 2025
PRIMARY
FDA UNII
772JOF6LZS
Created by admin on Mon Mar 31 19:24:57 GMT 2025 , Edited by admin on Mon Mar 31 19:24:57 GMT 2025
PRIMARY