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Details

Stereochemistry ACHIRAL
Molecular Formula C13H10O2
Molecular Weight 198.2173
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-HYDROXYBENZOPHENONE

SMILES

OC1=CC=C(C=C1)C(=O)C2=CC=CC=C2

InChI

InChIKey=NPFYZDNDJHZQKY-UHFFFAOYSA-N
InChI=1S/C13H10O2/c14-12-8-6-11(7-9-12)13(15)10-4-2-1-3-5-10/h1-9,14H

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Neutral, ion gas-phase energetics and structural properties of hydroxybenzophenones.
2010-04-16
A redetermination of 2-(6-diethyl-amino-3-diethyl-iminio-3H-xanthen-9-yl)benzoate-ethyl gallate (1/1) at room temperature.
2009-03-06
Simultaneous analysis of benzophenone sunscreen compounds in water sample by stir bar sorptive extraction with in situ derivatization and thermal desorption-gas chromatography-mass spectrometry.
2008-07-25
Toxicokinetics and metabolisms of benzophenone-type UV filters in rats.
2008-06-27
A low-temperature phase of the 1:1 complex of 2-(6-diethylamino-3-diethyl-iminio-3H-xanthen-9-yl)benzoate with ethyl gallate at 93 K.
2008-06-07
Determination of imatinib mesylate and its main metabolite (CGP74588) in human plasma and murine specimens by ion-pairing reversed-phase high-performance liquid chromatography.
2007-07
High-performance liquid chromatography analysis of curcumin in rat plasma: application to pharmacokinetics of polymeric micellar formulation of curcumin.
2007-05
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Simultaneous determination of benzophenone-type UV filters in water and soil by gas chromatography-mass spectrometry.
2006-10-27
Multiple hormonal activities of UV filters and comparison of in vivo and in vitro estrogenic activity of ethyl-4-aminobenzoate in fish.
2006-10-12
Expression profiling of estrogen-responsive genes in breast cancer cells treated with alkylphenols, chlorinated phenols, parabens, or bis- and benzoylphenols for evaluation of estrogenic activity.
2006-05-25
Comparison of in vitro and in vivo estrogenic activity of UV filters in fish.
2006-04
Development of a sensitive and specific liquid chromatography/mass spectrometry method for the quantification of cucurbitacin I (JSI-124) in rat plasma.
2006
Synthesis of benzoyl phenyl benzoates as effective inhibitors for phospholipase A2 and hyaluronidase enzymes.
2005-09-15
[Estrogenic activity of ultraviolet absorbers and the related compounds].
2005-08
Estrogenic and antiandrogenic activities of 17 benzophenone derivatives used as UV stabilizers and sunscreens.
2005-02-15
[Metabolic pathways of dipfluzine in rats].
2005-02
UV solvatochromic shifts of 4-hydroxy-benzophenone and 2,4-dihydroxy-benzophenone in ethanol-acetonitrile mixtures.
2003-11
Study of 202 natural, synthetic, and environmental chemicals for binding to the androgen receptor.
2003-10
Comparison of the reporter gene assay for ER-alpha antagonists with the immature rat uterotrophic assay of 10 chemicals.
2003-04-30
Immature rat uterotrophic assay of 18 chemicals and Hershberger assay of 30 chemicals.
2003-02-01
Benzophenone-induced estrogenic potency in ovariectomized rats.
2002-12
Genotoxic activation of benzophenone and its two metabolites by human cytochrome P450s in SOS/umu assay.
2002-08-26
Estrogenic potency of benzophenone and its metabolites in juvenile female rats.
2001-04
Patents
Name Type Language
NSC-1887
Preferred Name English
4-HYDROXYBENZOPHENONE
Systematic Name English
METHANONE, (4-HYDROXYPHENYL)PHENYL-
Systematic Name English
BENZOPHENONE, 4-HYDROXY-
Systematic Name English
P-BENZOYLPHENOL
Common Name English
(4-HYDROXYPHENYL)PHENYLMETHANONE
Systematic Name English
P-HYDROXYBENZOPHENONE
Common Name English
Code System Code Type Description
NSC
1887
Created by admin on Mon Mar 31 17:56:30 GMT 2025 , Edited by admin on Mon Mar 31 17:56:30 GMT 2025
PRIMARY
CAS
1137-42-4
Created by admin on Mon Mar 31 17:56:30 GMT 2025 , Edited by admin on Mon Mar 31 17:56:30 GMT 2025
PRIMARY
PUBCHEM
14347
Created by admin on Mon Mar 31 17:56:30 GMT 2025 , Edited by admin on Mon Mar 31 17:56:30 GMT 2025
PRIMARY
MESH
C024292
Created by admin on Mon Mar 31 17:56:30 GMT 2025 , Edited by admin on Mon Mar 31 17:56:30 GMT 2025
PRIMARY
FDA UNII
04R2LWS0MS
Created by admin on Mon Mar 31 17:56:30 GMT 2025 , Edited by admin on Mon Mar 31 17:56:30 GMT 2025
PRIMARY
ECHA (EC/EINECS)
214-507-1
Created by admin on Mon Mar 31 17:56:30 GMT 2025 , Edited by admin on Mon Mar 31 17:56:30 GMT 2025
PRIMARY
EPA CompTox
DTXSID5036684
Created by admin on Mon Mar 31 17:56:30 GMT 2025 , Edited by admin on Mon Mar 31 17:56:30 GMT 2025
PRIMARY