P22303
1-Phenyl-1-cyclohexene
95%
Sign In to View Organizational & Contract Pricing.
Select a Size
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%
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
Related Categories
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
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
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
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
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service