P22303
1-Phenyl-1-cyclohexene
95%
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About This Item
Formule linéaire :
C6H5C6H9
Numéro CAS:
Poids moléculaire :
158.24
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
Niveau de qualité
Pureté
95%
Indice de réfraction
n20/D 1.57 (lit.)
Point d'ébullition
251-253 °C (lit.)
Pf
−11 °C (lit.)
Densité
0.994 g/mL at 25 °C (lit.)
Chaîne 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
Clé InChI
WCMSFBRREKZZFL-UHFFFAOYSA-N
Code de la classe de stockage
10 - Combustible liquids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
217.4 °F - closed cup
Point d'éclair (°C)
103.00 °C - closed cup
Équipement de protection individuelle
Eyeshields, Gloves
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Les clients ont également consulté
A K Chaturvedi et al.
Pharmacology, biochemistry, and behavior, 30(4), 1035-1043 (1988-08-01)
The interaction between phencyclidine (PCP) and its pyrolysis product, 1-phenylcyclohexene (PC), at metabolic level was evaluated in Swiss male mice (21-24 g). PC (1.1, 2.2 and 4.4 mmol/kg/day for 4 days, IP, in corn oil) treatment to mice induced the
C Y Hu et al.
Toxicology and applied pharmacology, 76(3), 403-413 (1984-12-01)
The toxicity of 1-phenylcyclohexene (PC), a pyrolysis product of phencyclidine (PCP), and its interaction with PCP were evaluated. The ip LD50 of PC in Swiss male mice was 22 mmol/kg. Treatment of mice with PC at 2.2 mmol/kg/day, ip, for
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
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