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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

Molecular Formula C7H6O2
Molecular Weight 122.1213
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Continuous oxidation of aromatic aldehyde to aromatic carboxylic acid by Burkholderia cepacia TM1 in a cell-holding reactor.
2001
Flavonoids and aromatic compounds from the rhizomes of Zingiber zerumbet.
2004 Apr
The Hotdog fold: wrapping up a superfamily of thioesterases and dehydratases.
2004 Aug 12
A study of the spectral and redox properties and covalent flavinylation of the flavoprotein component of p-cresol methylhydroxylase reconstituted with FAD analogues.
2004 Aug 17
Estrogens and congeners from spent hops (Humulus lupulus).
2004 Dec
Anti-oxidative compounds in barley tea.
2004 Dec
Purification, crystallization and preliminary X-ray crystallographic analysis of hydroxycinnamoyl-coenzyme A hydratase-lyase (HCHL), a crotonase homologue active in phenylpropanoid metabolism.
2004 Dec
Chemical investigation and authenticity of Indian vanilla beans.
2004 Dec 15
A new anti-HIV alkaloid, drymaritin, and a new C-glycoside flavonoid, diandraflavone, from Drymaria diandra.
2004 Jul
Sonolysis of natural phenolic compounds in aqueous solutions: degradation pathways and biodegradability.
2004 Jul
Phenolic compounds and flavonoids as plant growth regulators from fruit and leaf of Vitex rotundifolia.
2004 Jul-Aug
Effect of binary combinations of selected toxic compounds on growth and fermentation of Kluyveromyces marxianus.
2004 May-Jun
Constituents of the stems of Macrococculus pomiferus and their inhibitory activities against cyclooxygenases-1 and -2.
2004 Nov
Metabolism of gallic acid and catechin by Lactobacillus hilgardii from wine.
2004 Oct 20
Profiling C6-C3 and C6-C1 phenolic metabolites in Cocos nucifera.
2005 Apr
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 Apr 20
Production of phleichrome by Cladosporium phlei as stimulated by diketopiperadines of Epichloe typhina.
2005 Aug
[Chemical constituents from tuber of Cremastra appendiculata].
2005 Dec
[Chemical constituents from leaves of Phyllostachys pubescens I].
2005 Dec
Bioactivation of 4-methylphenol (p-cresol) via cytochrome P450-mediated aromatic oxidation in human liver microsomes.
2005 Dec
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 Feb 24
Molecularly imprinted polymer with salicylaldehyde-Cu(OAc)2 as template.
2005 Jan-Feb
The 1.3 A crystal structure of the flavoprotein YqjM reveals a novel class of Old Yellow Enzymes.
2005 Jul 29
[Study on chemical constituents in seeds of Helicia nilagirica (II)].
2005 Jun
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 Jun
Synthesis and characterization of a novel functionalized azanonaborane cluster for boron neutron capture therapy.
2005 Jun 7
4-Hydroxybenzoyl derivative from the aqueous extract of the hydroid Campanularia sp.
2005 Mar
Longicalycinin A, a new cytotoxic cyclic peptide from Dianthus superbus var. longicalycinus (MAXIM.) WILL.
2005 Mar
Structure-function analysis of the vanillin molecule and its antifungal properties.
2005 Mar 9
[Study on chemical constituents in herbs of Anoectochilus roxburghii II].
2005 May
Two new sesquiterpenoids and anti-HIV principles from the root bark of Zanthoxylum ailanthoides.
2005 Nov 1
Antitubercular constituents from the stem wood of Cinnamomum kotoense.
2005 Sep
Synthesis of [13C]- and [14C]-labeled phenolic humus and lignin monomers.
2005 Sep
Transformation of Eutypa dieback and esca disease pathogen toxins by antagonistic fungal strains reveals a second detoxification pathway not present in Vitis vinifera.
2005 Sep 7
Acetalization and thioacetalization of cabonyl compounds: a case study based on global and local electrophilicity descriptors.
2006 Apr 30
A new cytotoxic amide from the stem wood of Hibiscus tiliaceus.
2006 Aug
Chemical fingerprint analysis of rhizomes of Gymnadenia conopsea by HPLC-DAD-MSn.
2006 Dec 5
COX-1, COX-2 inhibitors and antifungal agents from Croton hutchinsonianus.
2006 Feb
Anxiolytic-like effects of Gastrodia elata and its phenolic constituents in mice.
2006 Feb
Isolation and characterization of Halomonas sp. strain IMPC, a p-coumaric acid-metabolizing bacterium that decarboxylates other cinnamic acids under hypersaline conditions.
2006 Feb
Synthesis of Abyssinone II and related compounds as potential chemopreventive agents.
2006 Feb
Inhibition of GABA shunt enzymes' activity by 4-hydroxybenzaldehyde derivatives.
2006 Feb
Biotransformation of p-coumaric acid by Paecilomyces variotii.
2006 Jan
Inactivation of GABA transaminase by 4-acryloylphenol.
2006 Jul 15
Comparative analysis of iron regulated genes in mycobacteria.
2006 May 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 May 26
Quantitative determination of puerarin in dog plasma by HPLC and study on the relative bioavailability of sustained release tablets.
2006 May 3
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006 Nov
Degradation of phenolic compounds with hydrogen peroxide catalyzed by enzyme from Serratia marcescens AB 90027.
2006 Sep
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 Sep 22
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:28:36 GMT 2023
Edited
by admin
on Fri Dec 15 17:28:36 GMT 2023
Record UNII
O1738X3Y38
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-HYDROXYBENZALDEHYDE
FHFI  
Systematic 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
HYDROXYBENZALDEHYDE [INCI]
Common Name English
4-FORMYL PHENOL
Systematic Name English
HYDROXYBENZALDEHYDE
INCI  
INCI  
Official 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 Fri Dec 15 17:28:36 GMT 2023 , Edited by admin on Fri Dec 15 17:28:36 GMT 2023
Code System Code Type Description
MESH
C011483
Created by admin on Fri Dec 15 17:28:36 GMT 2023 , Edited by admin on Fri Dec 15 17:28:36 GMT 2023
PRIMARY
EPA CompTox
DTXSID8059552
Created by admin on Fri Dec 15 17:28:36 GMT 2023 , Edited by admin on Fri Dec 15 17:28:36 GMT 2023
PRIMARY
JECFA MONOGRAPH
889
Created by admin on Fri Dec 15 17:28:36 GMT 2023 , Edited by admin on Fri Dec 15 17:28:36 GMT 2023
PRIMARY
NSC
2127
Created by admin on Fri Dec 15 17:28:36 GMT 2023 , Edited by admin on Fri Dec 15 17:28:36 GMT 2023
PRIMARY
SMS_ID
100000143310
Created by admin on Fri Dec 15 17:28:36 GMT 2023 , Edited by admin on Fri Dec 15 17:28:36 GMT 2023
PRIMARY
WIKIPEDIA
4-HYDROXYBENZALDEHYDE
Created by admin on Fri Dec 15 17:28:36 GMT 2023 , Edited by admin on Fri Dec 15 17:28:36 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-599-1
Created by admin on Fri Dec 15 17:28:36 GMT 2023 , Edited by admin on Fri Dec 15 17:28:36 GMT 2023
PRIMARY
EVMPD
SUB119885
Created by admin on Fri Dec 15 17:28:36 GMT 2023 , Edited by admin on Fri Dec 15 17:28:36 GMT 2023
PRIMARY
CHEBI
24673
Created by admin on Fri Dec 15 17:28:36 GMT 2023 , Edited by admin on Fri Dec 15 17:28:36 GMT 2023
PRIMARY
MERCK INDEX
m6119
Created by admin on Fri Dec 15 17:28:36 GMT 2023 , Edited by admin on Fri Dec 15 17:28:36 GMT 2023
PRIMARY Merck Index
DRUG BANK
DB03560
Created by admin on Fri Dec 15 17:28:36 GMT 2023 , Edited by admin on Fri Dec 15 17:28:36 GMT 2023
PRIMARY
PUBCHEM
126
Created by admin on Fri Dec 15 17:28:36 GMT 2023 , Edited by admin on Fri Dec 15 17:28:36 GMT 2023
PRIMARY
CHEBI
17597
Created by admin on Fri Dec 15 17:28:36 GMT 2023 , Edited by admin on Fri Dec 15 17:28:36 GMT 2023
PRIMARY
FDA UNII
O1738X3Y38
Created by admin on Fri Dec 15 17:28:36 GMT 2023 , Edited by admin on Fri Dec 15 17:28:36 GMT 2023
PRIMARY
CAS
123-08-0
Created by admin on Fri Dec 15 17:28:36 GMT 2023 , Edited by admin on Fri Dec 15 17:28:36 GMT 2023
PRIMARY