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S4808

Sigma-Aldrich

cis-Stilbene

96%

Sinonimo/i:

cis-1,2-Diphenylethylene, Isostilbene

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About This Item

Formula condensata:
C6H5CH=CHC6H5
Numero CAS:
645-49-8
Peso molecolare:
180.25
Beilstein:
1616739
Numero CE:
211-445-7
Numero MDL:
MFCD00004788
Codice UNSPSC:
12352100
ID PubChem:
24899621
NACRES:
NA.22

Saggio

96%

Indice di rifrazione

n20/D 1.622 (lit.)

P. eboll.

82-84 °C/0.4 mmHg (lit.)

Densità

1.011 g/mL at 25 °C (lit.)

Temperatura di conservazione

2-8°C

Stringa SMILE

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-
PJANXHGTPQOBST-QXMHVHEDSA-N

Informazioni sul gene

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

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Categorie correlate

Descrizione generale

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.

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

230.0 °F - closed cup

Punto d’infiammabilità (°C)

110 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificati d'analisi (COA)

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Sigma-Aldrich

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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)
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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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
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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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