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Details

Stereochemistry ACHIRAL
Molecular Formula C7H6O4
Molecular Weight 154.1201
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,4-DIHYDROXYBENZOIC ACID

SMILES

OC(=O)C1=CC=C(O)C=C1O

InChI

InChIKey=UIAFKZKHHVMJGS-UHFFFAOYSA-N
InChI=1S/C7H6O4/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,8-9H,(H,10,11)

HIDE SMILES / InChI

Molecular Formula C7H6O4
Molecular Weight 154.1201
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Molecular cloning and characterization of a novel tomato xylosyltransferase specific for gentisic acid.
2010-10
Effect of subinhibitory concentrations of plant-derived molecules in increasing the sensitivity of multidrug-resistant Salmonella enterica serovar Typhimurium DT104 to antibiotics.
2010-10
Molecular modeling of peroxidase and polyphenol oxidase: substrate specificity and active site comparison.
2010-09-14
Bis(μ-2,4-dihy-droxy-benzoato-κO:O')bis-[aqua-(2,4-dihy-droxy-benzoato-κO)(1,10-phenanthroline-κN,N')cadmium(II)].
2010-06-09
beta-Resorcylic acid lactones from a Paecilomyces fungus.
2010-05-28
Bis(μ-4-chloro-2-oxidobenzoato)bis-[(1,10-phenanthroline)copper(II)] dihydrate.
2010-03-10
Hyperglycemia impairs proteasome function by methylglyoxal.
2010-03
Kinetics and Mechanisms of the Chromium(III) Reactions with 2,4- and 2,5-Dihydroxybenzoic Acids in Weak Acidic Aqueous Solutions.
2010
A study of oleic acid and 2,4-DHB acid aerosols using an IR-VUV-ITMS: insights into the strengths and weaknesses of the technique.
2009-09-28
Formation of bromoform in irradiated titanium dioxide suspensions with varying photocatalyst, dissolved organic carbon and bromide concentrations.
2009-09
Compatibility study of trans-1,4,5,8-tetranitro-1,4,5,8-tetraazadecalin (TNAD) with some energetic components and inert materials.
2008-12-30
Solid-state changes in ligand-to-metal charge-transfer spectra of (NH3)5Ru(III)(2,4-dihydroxybenzoate) and (NH3)5Ru(III)(xanthine) chromophores.
2008-11-03
Effect of the template and functional monomer on the textural properties of molecularly imprinted polymers.
2008-09-15
Cannabidiolic acid as a selective cyclooxygenase-2 inhibitory component in cannabis.
2008-09
Formation of brominated products in irradiated titanium dioxide suspensions containing bromide and dissolved organic carbon.
2008-03
DFT and ab initio study of structure of dyes derived from 2-hydroxy and 2,4-dihydroxy benzoic acids.
2008-02
2,4-Dihydr-oxy-N'-(4-methoxy-benzyl-idene)benzohydrazide.
2008-01-18
Inter-individual variability in esterases in human liver.
2007-09-15
Iron-doped carbon aerogels: novel porous substrates for direct growth of carbon nanotubes.
2007-04-24
Structure and hydrogen bonding in 2,4-dihydroxybenzoic acid at 90, 100, 110 and 150 K; a theoretical and single-crystal X-ray diffraction study.
2007-04
Chemistry and biology of resorcylic acid lactones.
2007-01-07
[Inhibitory effects of Lantana camera and its contained phenolic compounds in Eichhornia crassipes growth].
2006-09
Molecularly imprinted polymers with a streamlined mimic for zearalenone analysis.
2006-05-26
Determination of resorcylic acid lactones in biological samples by GC-MS. Discrimination between illegal use and contamination with fusarium toxins.
2006-03
Determination of aerobic-anaerobic metabolism-related compounds in a Chaoborus flavicans population by infusion ion trap mass spectrometry of extracts of individual larvae.
2006
Comparison of highly-fluorinated chloroformates as direct aqueous sample derivatizing agents for hydrophilic analytes and drinking-water disinfection by-products.
2005-06
Formation of graphitic structures in cobalt- and nickel-doped carbon aerogels.
2005-03-29
FT-IR and NMR spectroscopic studies of salicylic acid derivatives. II. Comparison of 2-hydroxy- and 2,4- and 2,5-dihydroxy derivatives.
2004-09
Antibacterial activities of naturally occurring compounds against antibiotic-resistant Bacillus cereus vegetative cells and spores, Escherichia coli, and Staphylococcus aureus.
2004-08
Beta-thujaplicin: new quantitative CZE method and adsorption to goethite.
2004-03-24
Influence of amide linkages on acidity determinations of humic substances Testing with model-mixtures.
2004-03-10
Improvements in ion signal reproducibility obtained using a homogeneous laser beam for on-line laser desorption/ionization of single particles.
2004
Altered balance of half-reactions in p-hydroxybenzoate hydroxylase caused by substituting the 2'-carbon of FAD with fluorine.
2003-06-20
Degradation products of cyanidin glycosides from tart cherries and their bioactivities.
2001-10
Kinetic model for phenolic compound oxidation by Fenton's reagent.
2001-10
Determination of calcium dobesilate in human plasma using ion-pairing extraction and high-performance liquid chromatography.
2001-05-05
Complexation equilibria and spectrophotometric determination of iron(III) with resorcylic acid.
2001-04-28
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:01:04 GMT 2025
Edited
by admin
on Mon Mar 31 19:01:04 GMT 2025
Record UNII
LU39SC9JYL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,4-DIHYDROXYBENZOIC ACID
FHFI  
Systematic Name English
.BETA.-RESORCYLIC ACID
MI  
Preferred Name English
2,4-DIHYDROXYBENZOIC ACID [FHFI]
Common Name English
BENZOIC ACID, 2,4-DIHYDROXY-
Common Name English
P-HYDROXYSALICYLIC ACID
Common Name English
COUPLER 320
Brand Name English
.BETA.-RESORCINOLIC ACID
Common Name English
NSC-4740
Code English
FEMA NO. 3798
Code English
4-CARBOXYRESORCINOL
Systematic Name English
4-HYDROXYSALICYLIC ACID
Systematic Name English
DIHYDROXYBENZOIC ACID, 2,4-
Common Name English
NSC-13564
Code English
.BETA.-RESORCYLIC ACID [MI]
Common Name English
Classification Tree Code System Code
JECFA EVALUATION 2,4-DIHYDROXYBENZOIC ACID
Created by admin on Mon Mar 31 19:01:04 GMT 2025 , Edited by admin on Mon Mar 31 19:01:04 GMT 2025
Code System Code Type Description
RXCUI
1368632
Created by admin on Mon Mar 31 19:01:04 GMT 2025 , Edited by admin on Mon Mar 31 19:01:04 GMT 2025
PRIMARY
WIKIPEDIA
2,4-DIHYDROXYBENZOIC ACID
Created by admin on Mon Mar 31 19:01:04 GMT 2025 , Edited by admin on Mon Mar 31 19:01:04 GMT 2025
PRIMARY
FDA UNII
LU39SC9JYL
Created by admin on Mon Mar 31 19:01:04 GMT 2025 , Edited by admin on Mon Mar 31 19:01:04 GMT 2025
PRIMARY
DAILYMED
LU39SC9JYL
Created by admin on Mon Mar 31 19:01:04 GMT 2025 , Edited by admin on Mon Mar 31 19:01:04 GMT 2025
PRIMARY
MERCK INDEX
m9548
Created by admin on Mon Mar 31 19:01:04 GMT 2025 , Edited by admin on Mon Mar 31 19:01:04 GMT 2025
PRIMARY Merck Index
NSC
4740
Created by admin on Mon Mar 31 19:01:04 GMT 2025 , Edited by admin on Mon Mar 31 19:01:04 GMT 2025
PRIMARY
JECFA MONOGRAPH
883
Created by admin on Mon Mar 31 19:01:04 GMT 2025 , Edited by admin on Mon Mar 31 19:01:04 GMT 2025
PRIMARY
EPA CompTox
DTXSID0025074
Created by admin on Mon Mar 31 19:01:04 GMT 2025 , Edited by admin on Mon Mar 31 19:01:04 GMT 2025
PRIMARY
PUBCHEM
1491
Created by admin on Mon Mar 31 19:01:04 GMT 2025 , Edited by admin on Mon Mar 31 19:01:04 GMT 2025
PRIMARY
NSC
13564
Created by admin on Mon Mar 31 19:01:04 GMT 2025 , Edited by admin on Mon Mar 31 19:01:04 GMT 2025
PRIMARY
DRUG BANK
DB02839
Created by admin on Mon Mar 31 19:01:04 GMT 2025 , Edited by admin on Mon Mar 31 19:01:04 GMT 2025
PRIMARY
CAS
89-86-1
Created by admin on Mon Mar 31 19:01:04 GMT 2025 , Edited by admin on Mon Mar 31 19:01:04 GMT 2025
PRIMARY
ECHA (EC/EINECS)
201-946-9
Created by admin on Mon Mar 31 19:01:04 GMT 2025 , Edited by admin on Mon Mar 31 19:01:04 GMT 2025
PRIMARY
SMS_ID
300000022711
Created by admin on Mon Mar 31 19:01:04 GMT 2025 , Edited by admin on Mon Mar 31 19:01:04 GMT 2025
PRIMARY
Related Record Type Details
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