Skip to Content
Merck
All Photos(1)

Documents

S4808

Sigma-Aldrich

cis-Stilbene

96%

Synonym(s):

cis-1,2-Diphenylethylene, Isostilbene

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
C6H5CH=CHC6H5
CAS Number:
645-49-8
Molecular Weight:
180.25
Beilstein:
1616739
EC Number:
211-445-7
MDL number:
MFCD00004788
UNSPSC Code:
12352100
PubChem Substance ID:
24899621
NACRES:
NA.22

Quality Level

100

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)

Looking for similar products? Visit Product Comparison Guide

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 Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service