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Merck

P22303

Sigma-Aldrich

1-Phenyl-1-cyclohexene

95%

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About This Item

Fórmula lineal:
C6H5C6H9
Número de CAS:
Peso molecular:
158.24
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22

Nivel de calidad

Ensayo

95%

índice de refracción

n20/D 1.57 (lit.)

bp

251-253 °C (lit.)

mp

−11 °C (lit.)

densidad

0.994 g/mL at 25 °C (lit.)

cadena SMILES

C1CCC(=CC1)c2ccccc2

InChI

1S/C12H14/c1-3-7-11(8-4-1)12-9-5-2-6-10-12/h1,3-4,7-9H,2,5-6,10H2

Clave InChI

WCMSFBRREKZZFL-UHFFFAOYSA-N

Código de clase de almacenamiento

10 - Combustible liquids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

217.4 °F - closed cup

Punto de inflamabilidad (°C)

103.00 °C - closed cup

Equipo de protección personal

Eyeshields, Gloves


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C E Cook et al.
Drug metabolism and disposition: the biological fate of chemicals, 12(2), 186-192 (1984-03-01)
In vitro metabolites of 1-phenylcyclohexene produced by the 10,000g supernatant fraction from rat liver homogenates were identified by a combination of spectrometric, chromatographic, and synthetic techniques. Initial oxidation occurred in the 3-position of 1-phenylcyclohexene to yield 1-phenyl-1-cyclohexen-3-one and 1-phenyl-1-cyclohexen-3-ol. Further
F C Law et al.
Drug and chemical toxicology, 7(3), 273-282 (1984-01-01)
The biliary excretion of 14C-phenylcyclohexene and its metabolites were studied in rats pretreated with an inducer or inhibitor of mixed-function oxidases or with an agent known to deplete liver glutathione. Pretreatment of rats with 3-methylcholanthrene or phenobarbital enhanced the biliary
A S Freeman et al.
Drug metabolism and disposition: the biological fate of chemicals, 10(6), 680-684 (1982-11-01)
Mice were exposed to the smoke from placebo marihuana cigarettes treated with phencyclidine hydrochloride (PCP . HCl). A dose-related decrement in motor performance was observed after exposure to the smoke from cigarettes containing 10-15 mg of PCP . HCl. Tissue
R L Beard et al.
Bioorganic & medicinal chemistry letters, 11(6), 765-768 (2001-03-30)
Retinoids are natural and synthetic analogues of the hormone retinoic acid. Systemic retinoid agonist therapy is usually associated with toxic side effects, such as mucocutaneous toxicity, which may be alleviated by the use of topical retinoid antagonists. We report the
D H Young et al.
Bioorganic & medicinal chemistry letters, 11(11), 1393-1396 (2001-05-30)
Phenylcyclohexenes (PCHs) [e.g., trans-4-nitro-5-(2,3,4-trimethoxyphenyl)cyclohexene, 2d] were found to bind weakly to the colchicine site of bovine tubulin, but are the first mimics of colchicine found to have high activity towards plant cells. Structure-activity relationships for PCHs and biphenyl AC-ring analogues

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