P22303
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
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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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Los clientes también vieron
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
B R Martin et al.
Drug metabolism and disposition: the biological fate of chemicals, 10(6), 685-689 (1982-11-01)
The in vitro metabolism of 1-3H-phenyl-1-cyclohexene (3H-PC) was studied in a crude microsomal preparation from mouse livers. The major routes of metabolism were allylic hydroxylation, oxidation of the allylic alcohol, and epoxidation-hydrolysis. The following metabolites were identified by comparison with
S Chakrabarti et al.
Toxicology and applied pharmacology, 69(2), 179-184 (1983-06-30)
The metabolic disposition of 1-[14C]phenylcyclohexene ([14C]PC) was examined in rats after ip or iv drug administration. Radioactivity, which was accumulated by various organs, peaked within 30 min after ip administration of [14C]PC (0.21 mg/kg). A significant amount of this radioactivity
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
A S Freeman et al.
Journal of pharmaceutical sciences, 70(9), 1002-1004 (1981-09-01)
Parsley cigarettes containing [3H]phencyclidine were machine smoked, and the mainstream smoke was trapped in glass wool filters. Radioactivity was extracted from these filters with chloroform. The average recoveries of radioactivity were 76, 85, 70, and 69% for cigarettes containing 3
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