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Details

Stereochemistry ACHIRAL
Molecular Formula C14H12
Molecular Weight 180.2451
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,1-DIPHENYLETHYLENE

SMILES

C=C(C1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=ZMYIIHDQURVDRB-UHFFFAOYSA-N
InChI=1S/C14H12/c1-12(13-8-4-2-5-9-13)14-10-6-3-7-11-14/h2-11H,1H2

HIDE SMILES / InChI

Molecular Formula C14H12
Molecular Weight 180.2451
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Dibenzofulvene, a 1,1-diphenylethylene analogue, gives a pi-stacked polymer by anionic, free-radical, and cationic catalysts.
2001 Sep 19
Asymmetric cyclopropanation catalyzed by a series of copper-(Schiff-base) complexes with two chiral centers.
2002 Nov-Dec
Electronically tuned chiral ruthenium porphyrins: extremely stable and selective catalysts for asymmetric epoxidation and cyclopropanation.
2003 Oct 6
Photodegradation of bisphenol-A with TiO2 immobilized on the glass tubes including the UV light lamps.
2004 Sep
Diastereoselective remote C-H activation by hydroboration.
2004 Sep 6
Synthesis, characterization, properties, and drug release of poly(alkyl methacrylate-b-isobutylene-b-alkyl methacrylate).
2006 Nov
Hydroaminomethylation with novel rhodium-carbene complexes: an efficient catalytic approach to pharmaceuticals.
2007
(E)-1,2-Bis{4-[dimeth-yl(vin-yl)silyl]-phenyl}-ethene.
2007 Dec 6
The thyroid disruptor 1,1,1-trichloro-2,2-bis(p-chlorophenyl)-ethane appears to be an uncompetitive inverse agonist for the thyrotropin receptor.
2007 Jan
Syntheses and structures of ytterbium(II) hydride and hydroxide complexes: similarities and differences with their calcium analogues.
2007 Jun 25
N-(Diphenyl-vinyl-idene)-2,6-diisopropyl-aniline.
2008 Dec 6
Convenient methods for preparing pi-conjugated linkers as building blocks for modular chemistry.
2009 Apr 14
1-Phenyl-1,2-cyclohexadiene: generation, interception by activated olefins, dimerisation and trimerisation.
2009 Oct 26
Mechanistic insight on the hydrogenation of conjugated alkenes with h(2) catalyzed by early main-group metal catalysts.
2010 Apr 5
Solvent and temperature effects on diastereodifferentiating Paternó-Büchi reaction of chiral alkyl cyanobenzoates with diphenylethene upon direct versus charge-transfer excitation.
2010 Aug 20
Synthesis and solution rheology of poly[(stearyl methacrylate)-stat-([2-(methacryloyloxy)ethyl] trimethyl ammonium iodide)].
2010 Nov 15
Controlling electron transfer in donor-bridge-acceptor molecules using cross-conjugated bridges.
2010 Nov 3
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:18:11 GMT 2023
Edited
by admin
on Fri Dec 15 15:18:11 GMT 2023
Record UNII
BX0L5B6LLL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,1-DIPHENYLETHYLENE
Systematic Name English
NSC-57645
Code English
.ALPHA.,.ALPHA.-DIPHENYLETHYLENE
Common Name English
1,1-DIPHENYLETHENE
MI  
Systematic Name English
ALPHA-PHENYLSTYRENE
Systematic Name English
ETHYLENE, 1,1-DIPHENYL
Common Name English
1'-ETHENYLIDENEBIS(BENZENE)
Common Name English
UNSYM-DIPHENYLETHYLENE
Common Name English
.ALPHA.-METHYLENE-DIPHENYLMETHANE
Common Name English
1,1-DIPHENYLETHENE [MI]
Common Name English
Code System Code Type Description
NSC
57645
Created by admin on Fri Dec 15 15:18:11 GMT 2023 , Edited by admin on Fri Dec 15 15:18:11 GMT 2023
PRIMARY
MERCK INDEX
m4626
Created by admin on Fri Dec 15 15:18:11 GMT 2023 , Edited by admin on Fri Dec 15 15:18:11 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
1,1-Diphenylethylene
Created by admin on Fri Dec 15 15:18:11 GMT 2023 , Edited by admin on Fri Dec 15 15:18:11 GMT 2023
PRIMARY
MESH
C007518
Created by admin on Fri Dec 15 15:18:11 GMT 2023 , Edited by admin on Fri Dec 15 15:18:11 GMT 2023
PRIMARY
PUBCHEM
10740
Created by admin on Fri Dec 15 15:18:11 GMT 2023 , Edited by admin on Fri Dec 15 15:18:11 GMT 2023
PRIMARY
CAS
530-48-3
Created by admin on Fri Dec 15 15:18:11 GMT 2023 , Edited by admin on Fri Dec 15 15:18:11 GMT 2023
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FDA UNII
BX0L5B6LLL
Created by admin on Fri Dec 15 15:18:11 GMT 2023 , Edited by admin on Fri Dec 15 15:18:11 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-482-6
Created by admin on Fri Dec 15 15:18:11 GMT 2023 , Edited by admin on Fri Dec 15 15:18:11 GMT 2023
PRIMARY
EPA CompTox
DTXSID5060190
Created by admin on Fri Dec 15 15:18:11 GMT 2023 , Edited by admin on Fri Dec 15 15:18:11 GMT 2023
PRIMARY