Vinyl Cyclohexene Reaction

Journal of analytical and applied pyrolysis 1988 13 4 259 275.

Vinyl cyclohexene reaction.

It is a precursor to vinylcyclohexene dioxide. Although chiral it is used mainly as the racemate. Compounds in this group react with acids bases and oxidizing and reducing agents. Benzene is converted to cyclohexylbenzene by acid catalyzed alkylation with cyclohexene.

4 vinyl 1 cyclohexene stabilized revision date 18 jan 2018 decomposition temperature no information available viscosity 0 7 mpa s at 20 c molecular formula c8 h12 molecular weight 108 18 10. The main 4 vinyl 1 cyclohexene metabolite formed in mice liver microsomes after incubation was 4 vinylcyclohexane 1 2 diol. It is produced by 1 3 butadiene dimerizes in a diels alder reaction. Rearrangement reactions in the thermal formation of aromatics from cycloolefins.

126 these processes occur with log k rac 12 09 49 650 2 3rt and. 1 vinyl 3 cyclohexene dioxide reacts with active hydrogen compounds such as alcohols and amines. It is soluble in water. 10 17 2016 en english us sds id.

4 vinylcyclohexene undergoes a retro diels alder reaction to butadiene with log k 15 2 62000 2 3rt 124 or 15 7 61 800 2 3rt. Epoxides are highly reactive. 4 vinylcyclohexene is an organic compound consisting of a vinyl group attached to the 4 position of the cyclohexene ring. Properties 4 vinyl 1 cyclohexene diepoxide is a colorless liquid at room temper ature ntp 1989.

They polymerize in the presence of catalysts or when heated. Take off immediately all contaminated clothing. Stability and reactivity reactive hazard none known based on information available stability stable under normal conditions. Conditions to avoid excess heat.

4 vinyl 1 cyclohexene safety data sheet print date. However it slowly hydrolyzes in aqueous solutions akron 2009. 4 vinyl 1 cyclohexene dioxide increased approx 10 times the forward mutation rate of v79 chinese hamster cells. These polymerization reactions can be violent.

Other metabolites were 4 vinyl 1 2 epoxycyclohexane 4 vinyl 1 cyclohexene dioxide. It is a colorless liquid. Cyclohexene is produced by the partial hydrogenation of benzene a process developed by the asahi chemical company. Use of the information documents and data from the echa website is subject to the terms and conditions of this legal notice and subject to other binding limitations provided for under applicable law the information documents and data made available on the echa website may be reproduced distributed and or used totally or in part for non commercial purposes provided that echa is.

Cyclohexylbenzene is a precursor to both phenol and cyclohexanone.