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

Details

Stereochemistry ACHIRAL
Molecular Formula C7H6O2
Molecular Weight 122.1213
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-HYDROXYBENZALDEHYDE

SMILES

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

InChI

InChIKey=RGHHSNMVTDWUBI-UHFFFAOYSA-N
InChI=1S/C7H6O2/c8-5-6-1-3-7(9)4-2-6/h1-5,9H

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Chemical fingerprint analysis of rhizomes of Gymnadenia conopsea by HPLC-DAD-MSn.
2006-12-05
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Ligand-induced conformational changes in the capping subdomain of a bacterial old yellow enzyme homologue and conserved sequence fingerprints provide new insights into substrate binding.
2006-09-22
Degradation of phenolic compounds with hydrogen peroxide catalyzed by enzyme from Serratia marcescens AB 90027.
2006-09
A new cytotoxic amide from the stem wood of Hibiscus tiliaceus.
2006-08
Inactivation of GABA transaminase by 4-acryloylphenol.
2006-07-15
Acid-promoted reaction of the stilbene antioxidant resveratrol with nitrite ions: mild phenolic oxidation at the 4'-hydroxystiryl sector triggering nitration, dimerization, and aldehyde-forming routes.
2006-05-26
Comparative analysis of iron regulated genes in mycobacteria.
2006-05-15
Quantitative determination of puerarin in dog plasma by HPLC and study on the relative bioavailability of sustained release tablets.
2006-05-03
Acetalization and thioacetalization of cabonyl compounds: a case study based on global and local electrophilicity descriptors.
2006-04-30
COX-1, COX-2 inhibitors and antifungal agents from Croton hutchinsonianus.
2006-02
Anxiolytic-like effects of Gastrodia elata and its phenolic constituents in mice.
2006-02
Isolation and characterization of Halomonas sp. strain IMPC, a p-coumaric acid-metabolizing bacterium that decarboxylates other cinnamic acids under hypersaline conditions.
2006-02
Synthesis of Abyssinone II and related compounds as potential chemopreventive agents.
2006-02
Inhibition of GABA shunt enzymes' activity by 4-hydroxybenzaldehyde derivatives.
2006-02
Biotransformation of p-coumaric acid by Paecilomyces variotii.
2006-01
[Chemical constituents from tuber of Cremastra appendiculata].
2005-12
[Chemical constituents from leaves of Phyllostachys pubescens I].
2005-12
Bioactivation of 4-methylphenol (p-cresol) via cytochrome P450-mediated aromatic oxidation in human liver microsomes.
2005-12
Two new sesquiterpenoids and anti-HIV principles from the root bark of Zanthoxylum ailanthoides.
2005-11-01
Transformation of Eutypa dieback and esca disease pathogen toxins by antagonistic fungal strains reveals a second detoxification pathway not present in Vitis vinifera.
2005-09-07
Antitubercular constituents from the stem wood of Cinnamomum kotoense.
2005-09
Synthesis of [13C]- and [14C]-labeled phenolic humus and lignin monomers.
2005-09
Production of phleichrome by Cladosporium phlei as stimulated by diketopiperadines of Epichloe typhina.
2005-08
The 1.3 A crystal structure of the flavoprotein YqjM reveals a novel class of Old Yellow Enzymes.
2005-07-29
Synthesis and characterization of a novel functionalized azanonaborane cluster for boron neutron capture therapy.
2005-06-07
[Study on chemical constituents in seeds of Helicia nilagirica (II)].
2005-06
Study on the bioavailability of puerarin from Pueraria lobata isoflavone self-microemulsifying drug-delivery systems and tablets in rabbits by liquid chromatography-mass spectrometry.
2005-06
[Study on chemical constituents in herbs of Anoectochilus roxburghii II].
2005-05
Identification and characterization of anthocyanins by high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry in common foods in the United States: vegetables, nuts, and grains.
2005-04-20
Phenolic compounds and flavonoids as plant growth regulators from fruit and leaf of Vitex rotundifolia.
2005-04-09
Profiling C6-C3 and C6-C1 phenolic metabolites in Cocos nucifera.
2005-04
Structure-function analysis of the vanillin molecule and its antifungal properties.
2005-03-09
4-Hydroxybenzoyl derivative from the aqueous extract of the hydroid Campanularia sp.
2005-03
Longicalycinin A, a new cytotoxic cyclic peptide from Dianthus superbus var. longicalycinus (MAXIM.) WILL.
2005-03
Synthesis and evaluation of double-prodrugs against HIV. Conjugation of D4T with 6-benzyl-1-(ethoxymethyl)-5-isopropyluracil (MKC-442, emivirine)-type reverse transcriptase inhibitors via the SATE prodrug approach.
2005-02-24
Chemical investigation and authenticity of Indian vanilla beans.
2004-12-15
Estrogens and congeners from spent hops (Humulus lupulus).
2004-12
Anti-oxidative compounds in barley tea.
2004-12
Purification, crystallization and preliminary X-ray crystallographic analysis of hydroxycinnamoyl-coenzyme A hydratase-lyase (HCHL), a crotonase homologue active in phenylpropanoid metabolism.
2004-12
Constituents of the stems of Macrococculus pomiferus and their inhibitory activities against cyclooxygenases-1 and -2.
2004-11
Metabolism of gallic acid and catechin by Lactobacillus hilgardii from wine.
2004-10-20
Molecularly imprinted polymer with salicylaldehyde-Cu(OAc)2 as template.
2004-09-24
A study of the spectral and redox properties and covalent flavinylation of the flavoprotein component of p-cresol methylhydroxylase reconstituted with FAD analogues.
2004-08-17
The Hotdog fold: wrapping up a superfamily of thioesterases and dehydratases.
2004-08-12
A new anti-HIV alkaloid, drymaritin, and a new C-glycoside flavonoid, diandraflavone, from Drymaria diandra.
2004-07
Sonolysis of natural phenolic compounds in aqueous solutions: degradation pathways and biodegradability.
2004-07
Effect of binary combinations of selected toxic compounds on growth and fermentation of Kluyveromyces marxianus.
2004-06-05
Flavonoids and aromatic compounds from the rhizomes of Zingiber zerumbet.
2004-04
Continuous oxidation of aromatic aldehyde to aromatic carboxylic acid by Burkholderia cepacia TM1 in a cell-holding reactor.
2001
Patents
Name Type Language
4-HYDROXYBENZALDEHYDE
FHFI  
Systematic Name English
HYDROXYBENZALDEHYDE
INCI  
INCI  
Preferred Name English
NSC-2127
Code English
FEMA NO. 3984
Code English
4-HYDROXYBENZALDEHYDE [FHFI]
Common Name English
4-FORMYLPHENOL
Systematic Name English
P-HYDROXYBENZALDEHYDE
MI  
Common Name English
PARAHYDROXYBENZALDEHYDE
Systematic Name English
4-FORMYL PHENOL
Systematic Name English
BENZALDEHYDE, 4-HYDROXY-
Systematic Name English
P-OXYBENZALDEHYDE
Common Name English
BISOPROLOL FUMARATE IMPURITY S [EP IMPURITY]
Common Name English
P-HYDROXYBENZALDEHYDE [MI]
Common Name English
Classification Tree Code System Code
JECFA EVALUATION 4-HYDROXYBENZALDEHYDE
Created by admin on Mon Mar 31 18:47:09 GMT 2025 , Edited by admin on Mon Mar 31 18:47:09 GMT 2025
Code System Code Type Description
MESH
C011483
Created by admin on Mon Mar 31 18:47:09 GMT 2025 , Edited by admin on Mon Mar 31 18:47:09 GMT 2025
PRIMARY
EPA CompTox
DTXSID8059552
Created by admin on Mon Mar 31 18:47:09 GMT 2025 , Edited by admin on Mon Mar 31 18:47:09 GMT 2025
PRIMARY
JECFA MONOGRAPH
889
Created by admin on Mon Mar 31 18:47:09 GMT 2025 , Edited by admin on Mon Mar 31 18:47:09 GMT 2025
PRIMARY
NSC
2127
Created by admin on Mon Mar 31 18:47:09 GMT 2025 , Edited by admin on Mon Mar 31 18:47:09 GMT 2025
PRIMARY
SMS_ID
100000143310
Created by admin on Mon Mar 31 18:47:09 GMT 2025 , Edited by admin on Mon Mar 31 18:47:09 GMT 2025
PRIMARY
WIKIPEDIA
4-HYDROXYBENZALDEHYDE
Created by admin on Mon Mar 31 18:47:09 GMT 2025 , Edited by admin on Mon Mar 31 18:47:09 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-599-1
Created by admin on Mon Mar 31 18:47:09 GMT 2025 , Edited by admin on Mon Mar 31 18:47:09 GMT 2025
PRIMARY
EVMPD
SUB119885
Created by admin on Mon Mar 31 18:47:09 GMT 2025 , Edited by admin on Mon Mar 31 18:47:09 GMT 2025
PRIMARY
CHEBI
24673
Created by admin on Mon Mar 31 18:47:09 GMT 2025 , Edited by admin on Mon Mar 31 18:47:09 GMT 2025
PRIMARY
MERCK INDEX
m6119
Created by admin on Mon Mar 31 18:47:09 GMT 2025 , Edited by admin on Mon Mar 31 18:47:09 GMT 2025
PRIMARY Merck Index
DRUG BANK
DB03560
Created by admin on Mon Mar 31 18:47:09 GMT 2025 , Edited by admin on Mon Mar 31 18:47:09 GMT 2025
PRIMARY
PUBCHEM
126
Created by admin on Mon Mar 31 18:47:09 GMT 2025 , Edited by admin on Mon Mar 31 18:47:09 GMT 2025
PRIMARY
CHEBI
17597
Created by admin on Mon Mar 31 18:47:09 GMT 2025 , Edited by admin on Mon Mar 31 18:47:09 GMT 2025
PRIMARY
FDA UNII
O1738X3Y38
Created by admin on Mon Mar 31 18:47:09 GMT 2025 , Edited by admin on Mon Mar 31 18:47:09 GMT 2025
PRIMARY
CAS
123-08-0
Created by admin on Mon Mar 31 18:47:09 GMT 2025 , Edited by admin on Mon Mar 31 18:47:09 GMT 2025
PRIMARY