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Merck
CN

S4808

cis-Stilbene

96%

Synonym(s):

cis-1,2-Diphenylethylene, Isostilbene

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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:
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Product Name

cis-Stilbene, 96%

InChI key

PJANXHGTPQOBST-QXMHVHEDSA-N

InChI

1S/C14H12/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-12H/b12-11-

SMILES string

c1ccc(cc1)\C=C/c2ccccc2

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

Quality Level

Gene Information

human ... ESR1(2099)
rat ... Esr1(24890)

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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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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)
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
Amani A Mahbub et al.
Anti-cancer agents in medicinal chemistry, 13(10), 1601-1613 (2013-06-26)
Mortality rates for leukemia are high despite considerable improvements in treatment. Since polyphenols exert pro-apoptotic effects in solid tumors, our study investigated the effects of polyphenols in haematological malignancies. The effect of eight polyphenols (quercetin, chrysin, apigenin, emodin, aloe-emodin, rhein
Hassan E Eldesouky et al.
Scientific reports, 10(1), 6089-6089 (2020-04-10)
Azole antifungals are vital therapeutic options for treating invasive mycotic infections. However, the emergence of azole-resistant isolates combined with limited therapeutic options presents a growing challenge in medical mycology. To address this issue, we utilized microdilution checkerboard assays to evaluate
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

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