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Detail of "31017-40-0"

  • CAS Number:
  • 31017-40-0
  • Name:
  • Benzene,cyclohexen-1-yl-

  • Molecular Structure:
  • Formula:
  • C12H14
  • Molecular Weight:
  • 158.24
  • Synonyms:
  • Benzene,cyclohexenyl- (6CI,7CI,8CI,9CI); Cyclohexenylbenzene; Phenylcyclohexene
  • EINECS:
  • 212-242-6
  • Density:
  • 0.994 g/mL at 25 °C(lit.)
  • Melting Point:
  • ?11 °C(lit.)
  • Boiling Point:
  • 251-253 °C(lit.)
  • Flash Point:
  • 218 °F
  • Safety:
  • 24/25 Details

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CAS No.31017-40-0 Benzene,cyclohexen-1-yl-

1-PHENYL-1-CYCLOHEXENE

Supplier:Dishman Europe Limited [ Select your country]

600Integral
600

Tel:44-207 323 0608

Address:120 New Cavendish Street

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CAS No.31017-40-0 Phenylcyclohexene

COLOR LESS LIQUID

Supplier:S.R.LABORATORIES [ India]

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Tel:914027177083

Address:HYDEARABAD

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CAS No.31017-40-0 1-PHENYL-1-CYCLOHEXENE

1-PHENYL-1-CYCLOHEXENE

Supplier:Gaylord Chemical Corporation [ United States]

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Tel:985 649 5464

Address:106 Galeria Blvd. Slidell, LA 70458

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CAS No.31017-40-0 Benzene,cyclohexen-1-yl-

Supplier:Dishman Europe Ltd. [ United Kingdom]

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610

Tel:+44 (0)207 323 0608

Address:Suite 4, De Walden Court, 85 New Cavendish Street London W1W 6XD, U.K.

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Reference

Effects of drug and chemical pretreatments on biliary excretion of phenylcyclohexene in the rat
Effects of drug and chemical pretreatments on biliary excretion of phenylcyclohexene in the rat. Law, F. C. P.; Chakrabarti, S. (Dep. Biol., Simon Fraser Univ., Burnaby, BC V5A 1S6, Can.). Drug Chem. Toxicol., 7(3), 273-82 (English) 1984. CODEN: DCTODJ. ISSN: 0148-0545. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) The biliary excretion of phenylcyclohexene (I) [31017-40-0], a pyrolysis product of phencyclidine, and its metabolites was studied in rats pretreated with an inducer or inhibitor of mixed-functioin oxidase [9040-60-2] or with an agent known to deplete liver glutathione [70-18-8]. Pretreatment of rats with 3-methylcholanthrene or phenobarbital enhanced the biliary excretion of phenylcyclohexene and(or) its metabolites. Conversely, pretreatment of rats with SKF-525A or piperonyl butoxide decreased the biliary excretion of pehnylcyclohexene and(or) its metabolites. In contrast, pretreatment of rats with diethylmaleate did not alter significantly the rate of biliary excretion of radioactivity.
Electronic structure of the polyacetylene film oriented by a liquid crystal solvent under magnetic field
Electronic structure of the polyacetylene film oriented by a liquid crystal solvent under magnetic field. Park, Yung Woo; Lee, Y. S.; Kim, Y. K.In this study, 25067-58-7 and 31017-40-0 are also used.; Lee, C. K.; Park, C.; Shirakawa, Hideki; Akagi, K.; Kitagaki, T.; Katayama, S. (Dep. Phys., Seoul Natl. Univ., Seoul 151, S. Korea). Synth. Met., 17(1-3), 539-44 (English) 1987. CODEN: SYMEDZ. ISSN: 0379-6779. DOCUMENT TYPE: Journal CA Section: 76 (Electric Phenomena) Section cross-reference(s): 36 The elec. transport properties of the liq. crystal and magnetic field oriented polyacetylene film are studied. FeCl3, SO3, I, and AsF5 are the dopants. The obsd. max. room temp. cond. is around 6000 W1 cm-1 with SO3 doped polyacetylene. High anisotropies of room-temp. cond. are obsd. for FeCl3, AsF5 and I-doped polyacetylenes indicating that the charge transfer is one dimensional in these polyacetylene derivs. However, in the case of SO3 doped polyacetylene, the anisotropy suggested that the interchain coupling is relatively strong. In thermopower data, no anisotropy is obsd., confirming that thermopower measures the intrinsic property of the polymer. The temp. dependence of cond. data of the FeCl3-doped polyacetylene indicates that there might be an elec. field effect and/or a structural rearrangement at <200 K. Quasi-linear temp. dependence of thermopower is obsd. for all dopants at high concn., showing the metallic nature of these heavily doped polyacetylenes. By comparing the thermopower data of AsF5- and SO3-doped polyacetylene to those of unoriented-polyacetylene films, the AsF5-doped oriented-polyacetylene shows slightly better crystallinity, and the SO3 doped oriented-polyacetylene shows a coupling between the chain and the dopant. .
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