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S4808

Sigma-Aldrich

cis-Stilbene

96%

Sinônimo(s):

cis-1,2-Diphenylethylene, Isostilbene

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About This Item

Fórmula linear:
C6H5CH=CHC6H5
Número CAS:
645-49-8
Peso molecular:
180.25
Beilstein:
1616739
Número CE:
211-445-7
Número MDL:
MFCD00004788
Código UNSPSC:
12352100
ID de substância PubChem:
24899621
NACRES:
NA.22

Ensaio

96%

índice de refração

n20/D 1.622 (lit.)

pb

82-84 °C/0.4 mmHg (lit.)

densidade

1.011 g/mL at 25 °C (lit.)

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

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-

chave InChI

PJANXHGTPQOBST-QXMHVHEDSA-N

Informações sobre genes

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

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Descrição geral

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.

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

230.0 °F - closed cup

Ponto de fulgor (°C)

110 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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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
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
Hassan E Eldesouky et al.
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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
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
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