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P22303

Sigma-Aldrich

1-Phenyl-1-Cyclohexen

95%

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About This Item

Lineare Formel:
C6H5C6H9
CAS-Nummer:
771-98-2
Molekulargewicht:
158.24
EG-Nummer:
212-242-6
MDL-Nummer:
MFCD00001542
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24898294
NACRES:
NA.22

Assay

95%

Brechungsindex

n20/D 1.57 (lit.)

bp

251-253 °C (lit.)

mp (Schmelzpunkt)

−11 °C (lit.)

Dichte

0.994 g/mL at 25 °C (lit.)

SMILES String

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

InChIKey

WCMSFBRREKZZFL-UHFFFAOYSA-N

Verwandte Kategorien

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

217.4 °F - closed cup

Flammpunkt (°C)

103.00 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves

Analysenzertifikate (COA)

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Brombenzen ≥99.5% (GC)

Sigma-Aldrich

16350

Brombenzen

α-Methylstyrol 99%, contains 15 ppm p-tert-butylcatechol as inhibitor

Sigma-Aldrich

M80903

α-Methylstyrol

Allylbenzol 98%

Sigma-Aldrich

A29402

Allylbenzol

4-Nitrotoluol 99%

Sigma-Aldrich

N27322

4-Nitrotoluol

Cyclohexenoxid 98%

Sigma-Aldrich

C102504

Cyclohexenoxid

Borandimethylsulfid-Komplex

Sigma-Aldrich

179825

Borandimethylsulfid-Komplex

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
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
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
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
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