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

Details

Stereochemistry ACHIRAL
Molecular Formula C13H12O
Molecular Weight 184.2338
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENZOHYDROL

SMILES

OC(C1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=QILSFLSDHQAZET-UHFFFAOYSA-N
InChI=1S/C13H12O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13-14H

HIDE SMILES / InChI

Molecular Formula C13H12O
Molecular Weight 184.2338
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Indoline-3-carboxylic acid derived organocatalysts for the anti-Mannich reaction.
2010-12-27
Undeca-carbonyl-1κC,2κC,3κC-[tris-(2-chloro-eth-yl) phosphite-1κP]-triangulo-triruthenium(0).
2010-09-04
Marine polysaccharides in pharmaceutical applications: an overview.
2010-09-02
Management of dyslipidemias with fibrates, alone and in combination with statins: role of delayed-release fenofibric acid.
2010-08-09
Undeca-carbonyl-1κC,2κC,3κC-{tris-[4-(methyl-sulfanyl)-phen-yl]arsine-1κAs}-triangulo-triruthenium(0).
2010-08-04
(2-Methyl-phen-yl)(phen-yl)methanol.
2010-07-31
Decacarbonyl-1κC,2κC,3κC-bis-[tris-(3-chloro-phen-yl)phosphine]-1κP,2κP-triangulo-triruthenium(0) monohydrate.
2010-04-28
Undeca-carbonyl-1κC,2κC,3κC-[tris-(3-chloro-phen-yl)phosphine-1κP]-triangulo-triruthenium(0).
2010-04-28
Undeca-carbonyl-1κC,2κC,3κC-[tris-(4-methyl-phen-yl)arsine-1κAs]-triangulo-triruthenium(0).
2009-11-21
Potent new small-molecule inhibitor of botulinum neurotoxin serotype A endopeptidase developed by synthesis-based computer-aided molecular design.
2009-11-10
Bioremediation of Bisphenol A and Benzophenone by Glycosylation with Immobilized Marine Microalga Pavlova sp.
2009-09-23
Improved tricyclic inhibitors of trypanothione reductase by screening and chemical synthesis.
2009-08
The use of molecular probes for the characterization of dispersions of functionalized silica nanoparticles.
2009-07
Time-resolved resonance Raman and density functional theory investigation of the photoreactions of benzophenone in aqueous solution.
2009-04-09
Asymmetric esterification of ketenes catalyzed by an N-heterocyclic carbene.
2009-01-21
Miniaturized hollow fiber assisted liquid-phase microextraction and gas chromatography-mass spectrometry for determination of benzophenone and derivates in human urine sample.
2009-01-15
Interaction of cocaine-, benztropine-, and GBR12909-like compounds with wild-type and mutant human dopamine transporters: molecular features that differentially determine antagonist-binding properties.
2008-11
Water-induced hydrophobicity of soy protein materials containing 2,2-diphenyl-2-hydroxyethanoic acid.
2008-09
Toxicokinetics and metabolisms of benzophenone-type UV filters in rats.
2008-06-27
Structural and spectroscopic characterization of a charge-separated uranium benzophenone ketyl radical complex.
2008-05-21
Measurement of benzophenones in human urine samples by stir bar sorptive extraction and thermal desorption-gas chromatography-mass spectrometry.
2008
Covalent sidewall functionalization of single-walled carbon nanotubes: a photoreduction approach.
2007-12-12
Time-resolved resonance Raman identification and structural characterization of a light absorbing transient intermediate in the photoinduced reaction of benzophenone in 2-propanol.
2007-09-14
The Mg-oppenauer oxidation as a mild method for the synthesis of aryl and metallocenyl ketones.
2007
Simultaneous determination of benzophenone-type UV filters in water and soil by gas chromatography-mass spectrometry.
2006-10-27
Comparative structure-activity relationships of benztropine analogues at the dopamine transporter and histamine H(1) receptors.
2006-06-01
Enhancement of chain amplification in photoreactions of N-methoxypyridinium salts with alcohols.
2005-09-24
Reduction of benzophenone by SmI2: the role of proton donors in determining product distribution.
2005-09-15
Chain amplification in photoreactions of N-alkoxypyridinium salts with alcohols: mechanism and kinetics.
2005-08-19
[Estrogenic activity of ultraviolet absorbers and the related compounds].
2005-08
[Metabolic pathways of dipfluzine in rats].
2005-02
Towards a total synthesis of the new anticancer agent mensacarcin: synthesis of the carbocyclic core.
2004-10-11
New 4-[omega-(diarylmethylamino)alkyl]- and 4-[omega-(diarylmethoxy)alkyl]-1-arylpiperazines as selective 5-HT1A/5-HT2A receptor ligands with differentiated in vivo activity.
2004-07-19
Identification of diphenhydramine metabolites in human urine by capillary electrophoresis-ion trap-mass spectrometry.
2004-06
Mutation of Trp84 and Asp313 of the dopamine transporter reveals similar mode of binding interaction for GBR12909 and benztropine as opposed to cocaine.
2004-05
Comparative pharmacokinetics of diphenhydramine in camels and horses after intravenous administration.
2003-09
Novel 4-alkyl-1-arylpiperazines and 1,2,3,4-tetrahydroisoquinolines containing diphenylmethylamino or diphenylmethoxy fragment with differentiated 5-HT1A/5-HT2A/D2 receptor activity.
2003-05-26
Monitoring the formation and decay of transient photosensitized intermediates using pump-probe UV resonance Raman spectroscopy. II: Kinetic modeling and multidimensional least-squares analysis.
2003-04
Monitoring the formation and decay of transient photosensitized intermediates using pump-probe UV resonance Raman spectroscopy. I: Self-modeling curve resolution.
2003-04
Tuning copper-dioxygen reactivity and exogenous substrate oxidations via alterations in ligand electronics.
2003-01-22
Benzophenone-induced estrogenic potency in ovariectomized rats.
2002-12
Biotransformation of cyclizine in greyhounds. 2: N(1)-dealkylation and identification of some neutral and phenolic metabolites in canine urine by gas chromatography-mass spectrometry.
2002-09
Genotoxic activation of benzophenone and its two metabolites by human cytochrome P450s in SOS/umu assay.
2002-08-26
Photoreduction of benzophenones by amines in room-temperature ionic liquids.
2002-03-21
Estrogenic potency of benzophenone and its metabolites in juvenile female rats.
2001-04
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:09:58 GMT 2025
Edited
by admin
on Mon Mar 31 19:09:58 GMT 2025
Record UNII
S4HQ1H8OWD
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BENZOHYDROL
MI  
Common Name English
BENZHYDROL
USP-RS  
Preferred Name English
NSC-32150
Code English
DIMENHYDRINATE IMPURITY I [EP IMPURITY]
Common Name English
DIPHENHYDRAMINE HYDROCHLORIDE IMPURITY D [EP IMPURITY]
Common Name English
DIMENHYDRINATE IMPURITY I
EP  
Common Name English
BENZHYDROL [USP-RS]
Common Name English
DIPHENHYDRAMINE IMPURITY D
Common Name English
BENZOHYDROL [MI]
Common Name English
BENZHYDROL [USP IMPURITY]
Common Name English
DIPHENYLCARBINOL
Systematic Name English
Code System Code Type Description
CAS
91-01-0
Created by admin on Mon Mar 31 19:09:58 GMT 2025 , Edited by admin on Mon Mar 31 19:09:58 GMT 2025
PRIMARY
MERCK INDEX
m2362
Created by admin on Mon Mar 31 19:09:58 GMT 2025 , Edited by admin on Mon Mar 31 19:09:58 GMT 2025
PRIMARY Merck Index
WIKIPEDIA
Diphenylmethanol
Created by admin on Mon Mar 31 19:09:58 GMT 2025 , Edited by admin on Mon Mar 31 19:09:58 GMT 2025
PRIMARY
PUBCHEM
7037
Created by admin on Mon Mar 31 19:09:58 GMT 2025 , Edited by admin on Mon Mar 31 19:09:58 GMT 2025
PRIMARY
EPA CompTox
DTXSID2059015
Created by admin on Mon Mar 31 19:09:58 GMT 2025 , Edited by admin on Mon Mar 31 19:09:58 GMT 2025
PRIMARY
RS_ITEM_NUM
1051602
Created by admin on Mon Mar 31 19:09:58 GMT 2025 , Edited by admin on Mon Mar 31 19:09:58 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-033-8
Created by admin on Mon Mar 31 19:09:58 GMT 2025 , Edited by admin on Mon Mar 31 19:09:58 GMT 2025
PRIMARY
MESH
C020225
Created by admin on Mon Mar 31 19:09:58 GMT 2025 , Edited by admin on Mon Mar 31 19:09:58 GMT 2025
PRIMARY
CHEBI
156087
Created by admin on Mon Mar 31 19:09:58 GMT 2025 , Edited by admin on Mon Mar 31 19:09:58 GMT 2025
PRIMARY
FDA UNII
S4HQ1H8OWD
Created by admin on Mon Mar 31 19:09:58 GMT 2025 , Edited by admin on Mon Mar 31 19:09:58 GMT 2025
PRIMARY
NSC
32150
Created by admin on Mon Mar 31 19:09:58 GMT 2025 , Edited by admin on Mon Mar 31 19:09:58 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> METABOLITE
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (GC)
USP