Vinyl Cyclohexene Reaction

Conditions to avoid excess heat.

Vinyl cyclohexene reaction.

Cyclohexene is produced by the partial hydrogenation of benzene a process developed by the asahi chemical company. Although chiral it is used mainly as the racemate. 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. 1 vinyl 3 cyclohexene dioxide reacts with active hydrogen compounds such as alcohols and amines.

Other metabolites were 4 vinyl 1 2 epoxycyclohexane 4 vinyl 1 cyclohexene dioxide. 4 vinyl 1 cyclohexene dioxide increased approx 10 times the forward mutation rate of v79 chinese hamster cells. It is a precursor to vinylcyclohexene dioxide. It is produced by 1 3 butadiene dimerizes in a diels alder reaction.

4 vinylcyclohexene is an organic compound consisting of a vinyl group attached to the 4 position of the cyclohexene ring. Rearrangement reactions in the thermal formation of aromatics from cycloolefins. 4 vinyl 1 cyclohexene safety data sheet print date. Journal of analytical and applied pyrolysis 1988 13 4 259 275.

Stability and reactivity reactive hazard none known based on information available stability stable under normal conditions. 125 at lower temperatures optically active 4 exo dideuteriovinyl cyclohexene undergoes both racemization and deuterium scrambling to c 3. The main 4 vinyl 1 cyclohexene metabolite formed in mice liver microsomes after incubation was 4 vinylcyclohexane 1 2 diol. Cyclohexylbenzene is a precursor to both phenol and cyclohexanone.

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. Physical and chemical properties of 4 vinyl 1 cyclohexene diepoxide are listed in the following table. These polymerization reactions can be violent. Enev4520 2 8 p273 avoid release to the environment p303 p361 p353 if on skin or hair.

126 these processes occur with log k rac 12 09 49 650 2 3rt and. It is soluble in water. Compounds in this group react with acids bases and oxidizing and reducing agents. It is a colorless liquid.

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. 10 17 2016 en english us sds id. They polymerize in the presence of catalysts or when heated. Take off immediately all contaminated clothing.

However it slowly hydrolyzes in aqueous solutions akron 2009.