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Details

Stereochemistry ACHIRAL
Molecular Formula C13H10O3
Molecular Weight 214.2167
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4,4'-DIHYDOXY-BENZOPHENONE

SMILES

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

InChI

InChIKey=RXNYJUSEXLAVNQ-UHFFFAOYSA-N
InChI=1S/C13H10O3/c14-11-5-1-9(2-6-11)13(16)10-3-7-12(15)8-4-10/h1-8,14-15H

HIDE SMILES / InChI

Molecular Formula C13H10O3
Molecular Weight 214.2167
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
4-(4-Hydroxybenzoyl)phenol mono-hydrate.
2010-10-20
X-ray structure of 4,4'-dihydroxybenzophenone mimicking sterol substrate in the active site of sterol 14alpha-demethylase (CYP51).
2008-05-30
Convenient one-pot synthesis of 2,2-bis-(4-hydroxyphenyl)-cyclopentanone.
2008-01-18
Degradation of Bis(4-Hydroxyphenyl)methane (bisphenol F) by Sphingobium yanoikuyae strain FM-2 isolated from river water.
2008-01
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Fluorine-substituted cyclofenil derivatives as estrogen receptor ligands: synthesis and structure-affinity relationship study of potential positron emission tomography agents for imaging estrogen receptors in breast cancer.
2006-04-20
Biodegradation of a variety of bisphenols under aerobic and anaerobic conditions.
2006
Estrogenic and antiandrogenic activities of 17 benzophenone derivatives used as UV stabilizers and sunscreens.
2005-02-15
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
Effect of ultraviolet light absorbers on photostabilization of azadirachtin-A in solution (part: II).
2003-01
Effect of some ultraviolet light absorbers on photo-stabilization of azadirachtin-A.
2002-10
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:34:53 GMT 2025
Edited
by admin
on Mon Mar 31 20:34:53 GMT 2025
Record UNII
HZR7D31SBY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-2831
Preferred Name English
4,4'-DIHYDOXY-BENZOPHENONE
Common Name English
BIS(4-HYDROXYPHENYL)METHANONE
Systematic Name English
4,4'DIHYDROXYBENZOPHENONE
Systematic Name English
METHANONE, BIS(4-HYDROXYPHENYL)-
Systematic Name English
BIS(4-HYDROXYPHENYL) KETONE
Systematic Name English
P,P'-DIHYDROXYBENZOPHENONE
Common Name English
4,4'-DIHYDROXYBENZOPHENONE
Systematic Name English
Code System Code Type Description
FDA UNII
HZR7D31SBY
Created by admin on Mon Mar 31 20:34:53 GMT 2025 , Edited by admin on Mon Mar 31 20:34:53 GMT 2025
PRIMARY
EPA CompTox
DTXSID1022425
Created by admin on Mon Mar 31 20:34:53 GMT 2025 , Edited by admin on Mon Mar 31 20:34:53 GMT 2025
PRIMARY
CAS
611-99-4
Created by admin on Mon Mar 31 20:34:53 GMT 2025 , Edited by admin on Mon Mar 31 20:34:53 GMT 2025
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NSC
2831
Created by admin on Mon Mar 31 20:34:53 GMT 2025 , Edited by admin on Mon Mar 31 20:34:53 GMT 2025
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WIKIPEDIA
4,4'-Dihydroxybenzophenone
Created by admin on Mon Mar 31 20:34:53 GMT 2025 , Edited by admin on Mon Mar 31 20:34:53 GMT 2025
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DRUG BANK
DB07635
Created by admin on Mon Mar 31 20:34:53 GMT 2025 , Edited by admin on Mon Mar 31 20:34:53 GMT 2025
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ECHA (EC/EINECS)
210-288-1
Created by admin on Mon Mar 31 20:34:53 GMT 2025 , Edited by admin on Mon Mar 31 20:34:53 GMT 2025
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PUBCHEM
69150
Created by admin on Mon Mar 31 20:34:53 GMT 2025 , Edited by admin on Mon Mar 31 20:34:53 GMT 2025
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