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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
Synthesis and catalytic antibody functionalization of dendrimers.
2001 Aug 29
In vitro effects of hydroxybenzaldehydes from Gastrodia elata and their analogues on GABAergic neurotransmission, and a structure-activity correlation.
2001 Dec
Effects of noncovalent and covalent FAD binding on the redox and catalytic properties of p-cresol methylhydroxylase.
2001 Feb 20
Rerouting the plant phenylpropanoid pathway by expression of a novel bacterial enoyl-CoA hydratase/lyase enzyme function.
2001 Jul
Simultaneous determination of p-hydroxybenzaldehyde, p-hydroxybenzyl alcohol, 4-(beta-D-glucopyranosyloxy)-benzyl alcohol, and sugars in Gastrodia elata blume measured as their acetylated derivatives by GC-MS.
2001 Jun
Diterpenes and other constituents from Croton draco (Euphorbiaceae).
2001 Mar
Tyrosine and phenylalanine catabolism by Lactobacillus cheese flavor adjuncts.
2001 May
Daucane phytoestrogens: a structure-activity study.
2002 Nov
Induction of laccase activity in the edible straw mushroom, Volvariella volvacea.
2003 Jan 21
Antioxidant constituents from the stem of Sorghum bicolor.
2003 Jul
Purification of bioethanol effluent in an UASB reactor system with simultaneous biogas formation.
2003 Oct 5
Application of solid-phase extraction for determination of phenolic compounds in barrique wines.
2003 Sep
Flavonoids and aromatic compounds from the rhizomes of Zingiber zerumbet.
2004 Apr
Estrogens and congeners from spent hops (Humulus lupulus).
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
Phelligridins C-F: cytotoxic pyrano[4,3-c][2]benzopyran-1,6-dione and furo[3,2-c]pyran-4-one derivatives from the fungus Phellinus igniarius.
2004 May
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
Bioactivation of 4-methylphenol (p-cresol) via cytochrome P450-mediated aromatic oxidation in human liver microsomes.
2005 Dec
The 1.3 A crystal structure of the flavoprotein YqjM reveals a novel class of Old Yellow Enzymes.
2005 Jul 29
Synthesis and characterization of a novel functionalized azanonaborane cluster for boron neutron capture therapy.
2005 Jun 7
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
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
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
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006 Nov
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