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About This Item
Linear Formula:
C6H5CH=CHC6H5
CAS Number:
Molecular Weight:
180.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-445-7
Beilstein/REAXYS Number:
1616739
MDL number:
Assay:
96%
Quality Level
assay
96%
refractive index
n20/D 1.622 (lit.)
bp
82-84 °C/0.4 mmHg (lit.)
density
1.011 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
c1ccc(cc1)\C=C/c2ccccc2
InChI
1S/C14H12/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-12H/b12-11-
InChI key
PJANXHGTPQOBST-QXMHVHEDSA-N
Gene Information
human ... ESR1(2099)
rat ... Esr1(24890)
General description
cis-Stilbene can undergo epoxidation in the presence of supported gold nanoparticles (AuNP) and using cumene as a solvent to form a mixture of cis- and trans-stilbene oxides.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Daniel T Bregante et al.
Journal of the American Chemical Society, 139(20), 6888-6898 (2017-04-30)
Group IV and V framework-substituted zeolites have been used for olefin epoxidation reactions for decades, yet the underlying properties that determine the selectivities and turnover rates of these catalysts have not yet been elucidated. Here, a combination of kinetic, thermodynamic
Jana L van den Berg et al.
The journal of physical chemistry. A, 124(29), 5999-6008 (2020-06-26)
Previously, it has been demonstrated that external electric fields may be used to exert control over chemical reactivity. In this study, the impact of a strong, nonresonant IR field (1064 nm) on the photoisomerization of cis-stilbene is investigated in cyclohexane
Epoxidation of stilbene using supported gold nanoparticles: cumyl peroxyl radical activation at the gold nanoparticle surface.
Crites COL, et al.
Chemical Communications (Cambridge, England), 50(18), 2289-2291 (2014)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| S4808-10G | 04061838355645 |
| S4808-1G | 04061836931841 |
| S4808-5G | 04061836932084 |