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Merck
CN

P22303

1-Phenyl-1-cyclohexene

95%

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About This Item

Linear Formula:
C6H5C6H9
CAS Number:
Molecular Weight:
158.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
212-242-6
MDL number:
Assay:
95%
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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

InChI key

WCMSFBRREKZZFL-UHFFFAOYSA-N

SMILES string

C1CCC(=CC1)c2ccccc2

assay

95%

refractive index

n20/D 1.57 (lit.)

bp

251-253 °C (lit.)

mp

−11 °C (lit.)

density

0.994 g/mL at 25 °C (lit.)

Quality Level

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

217.4 °F - closed cup

flash_point_c

103.00 °C - closed cup

ppe

Eyeshields, Gloves


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C E Cook et al.
Clinical pharmacology and therapeutics, 31(5), 635-641 (1982-05-01)
Five men who smoked parsley cigarettes containing 100 micrograms of [3H]-phencyclidine hydrochloride (PCP.HCl) inhaled 69 +/- 5(SEM) % of the total radioactivity in the cigarette. Both PCP and its pyrolysis product, 1-phenylcyclohexene (PC), were found and measured in plasma. Calculations
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
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

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