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D206806

Sigma-Aldrich

1,1-Diphenylethylene

97%

Synonym(s):

α,α-Diphenylethylene, 1,1-Diphenylethene, 1,1′-Ethenylidenebis[benzene], 1-Phenylethenylbenzene, Rhodium acetate

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About This Item

Linear Formula:
(C6H5)2C=CH2
CAS Number:
530-48-3
Molecular Weight:
180.25
Beilstein/REAXYS Number:
1099062
EC Number:
208-482-6
MDL number:
MFCD00008583
UNSPSC Code:
12352100
PubChem Substance ID:
24893616
NACRES:
NA.22

assay

97%

form

liquid

refractive index

n20/D 1.608 (lit.)

bp

270-271 °C (lit.)

mp

6 °C (lit.)

density

1.021 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

C=C(c1ccccc1)c2ccccc2

InChI

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

InChI key

ZMYIIHDQURVDRB-UHFFFAOYSA-N

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pictograms

Environment
GHS09

hcodes

H411

Hazard Classifications

Aquatic Chronic 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves

Certificates of Analysis (COA)

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E Bignon et al.
Biochemical and biophysical research communications, 166(3), 1471-1478 (1990-02-14)
Protein kinase C (PKC) I (gamma), II (beta) and III (alpha) subspecies are all activated by 1,1-di-(p-hydroxyphenyl)ethylene derivatives (DPE) at micromolar concentrations. This PKC activation depends on the presence of both Ca2+ and phosphatidylserine (PS) but does not require diacylglycerol
Hongru Li et al.
Journal of fluorescence, 21(4), 1721-1728 (2011-03-04)
This article presents a comprehensive theoretical investigation of excited state intramolecular proton transfer (ESIPT) for some newly-designed diphenylethylene derivatives containing 2-(2-hydroxy-phenyl)-benzotriazole moiety with various substituted groups. The calculation shows the structural parameters and Mulliken charges of phototautomers enol (E) and
Moballigh Ahmed et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 13(5), 1594-1601 (2006-11-09)
Starting from [{Rh(cod)Cl}(2)] and 1,3-dimesitylimidazole-2-ylidenes the novel [RhCl(cod)(carbene)] complexes 1-5 have been synthesized, characterized, and tested in the hydroaminomethylation of aromatic olefins. The influence of different ligands and reaction parameters on the catalytic activity was investigated in detail applying 1,1-diphenylethylene
Debajyoti Ray et al.
Environmental science & technology, 45(23), 10061-10067 (2011-11-11)
We measured the kinetics of ozonation reaction of 1,1-diphenylethylene (DPE) in artificial snow, produced by shock freezing of DPE aqueous solutions sprayed into liquid nitrogen. It was demonstrated that most of the reactant molecules are in direct (productive) contact with
C Strömpl et al.
Archives of environmental contamination and toxicology, 33(4), 350-356 (1998-01-31)
Bacterial degradation of 1,1-dichloro-2,2-bis-(4-chlorophenyl)-ethylene (DDE) and its dehalogenated derivative 1,1-diphenylethylene (DPE) has not yet been shown and may require culture adaptation and special culture conditions. We compared the degradability of DPE, DDE, and pentachlorophenol (PCP) in aerobic/anaerobic sequenced batch reactor
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