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P22303

1-Phenyl-1-cyclohexene

Name: 1-Phenyl-1-cyclohexene
Brand: ALDRICH

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About This Item

Linear Formula:

C₆H₅C₆H₉

CAS Number:

771-98-2

Molecular Weight:

158.24

NACRES:

NA.22

PubChem Substance ID:

24898294

UNSPSC Code:

12352100

EC Number:

212-242-6

MDL number:

MFCD00001542

Assay:

95%

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Properties

Quality Level

100

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.)

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

InChI key

WCMSFBRREKZZFL-UHFFFAOYSA-N

Description

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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Phenylcyclohexene and phenylcyclohexadiene substituted compounds having retinoid antagonist activity.

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

Structure-activity relationships of phenylcyclohexene and biphenyl antitubulin compounds against plant and mammalian cells.

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

In vitro metabolism of 1-phenyl-1-cyclohexene, a pyrolysis product of phencyclidine.

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

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Global Trade Item Number

SKU	GTIN
P22303-5G	04061834362777
P22303-25G	04061833392416