4-Vinylcyclohexene is an organic compound consisting of a vinyl group attached to the 4-position of the cyclohexene ring. It is a colorless liquid. Although chiral, it is used mainly as the racemate. It is a precursor to vinylcyclohexene dioxide. [4]

Vinylcyclohexene | C8H12 | CID 17497 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

4-Vinylcyclohexene is produced by catalytic dimerization of 1,3-butadiene. 4-Vinylcyclohexene has been used as a chemical intermediate for production of flame retardants, flavours and fragrances, in the manufacture of polyolefins, as a solvent and in the manufacture of its diepoxide.

4-Vinylcyclohexene | C6H9CH=CH2 or C8H12 | CID 7499 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

VINYLCYCLOHEXENE can react with oxidizing materials. It is also incompatible with peroxide catalysts. Prolonged exposure to oxygen-containing gases leads to discoloration and gum formation.

2020年12月15日 · ACGIH: Documentation of the Threshold Limit Values (TLVs) and Biological Exposure Indices (BEIs) - 4-Vinyl cyclohexene. See annual publication for most recent information.

4-Vinylcyclohexene (VCH) is a derivative of 1,3-butadiene, an industrial compound used as a solvent in the synthesis of polymers, resins, plasticizers, and flame retardants. Both VCH and its metabolite VCD have been well characterized for their ovotoxicity ( …

Stereochemical aspects in the 4-vinylcyclohexene biotransformation with rat liver microsomes and purified cytochrome P450s: diepoxide formation and hydrolysis.

ChemSpider record containing structure, synonyms, properties, vendors and database links for Vinylcyclohexene, 2622-21-1, SDRZFSPCVYEJTP-UHFFFAOYSA-N

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