Vinyl Cyclohexene Reaction

Properties 4 vinyl 1 cyclohexene diepoxide is a colorless liquid at room temper ature ntp 1989.

Vinyl cyclohexene reaction.

Journal of analytical and applied pyrolysis 1988 13 4 259 275. It is a precursor to vinylcyclohexene dioxide. The main 4 vinyl 1 cyclohexene metabolite formed in mice liver microsomes after incubation was 4 vinylcyclohexane 1 2 diol. Conditions to avoid excess heat.

Epoxides are highly reactive. Although chiral it is used mainly as the racemate. 4 vinyl 1 cyclohexene safety data sheet print date. It is a colorless liquid.

125 at lower temperatures optically active 4 exo dideuteriovinyl cyclohexene undergoes both racemization and deuterium scrambling to c 3. It is soluble in water. Take off immediately all contaminated clothing. 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.

4 vinylcyclohexene is an organic compound consisting of a vinyl group attached to the 4 position of the cyclohexene ring. Other metabolites were 4 vinyl 1 2 epoxycyclohexane 4 vinyl 1 cyclohexene dioxide. Stability and reactivity reactive hazard none known based on information available stability stable under normal conditions. Physical and chemical properties of 4 vinyl 1 cyclohexene diepoxide are listed in the following table.

10 17 2016 en english us sds id. Cyclohexene is produced by the partial hydrogenation of benzene a process developed by the asahi chemical company. 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. 126 these processes occur with log k rac 12 09 49 650 2 3rt and.

It is produced by 1 3 butadiene dimerizes in a diels alder reaction. Rearrangement reactions in the thermal formation of aromatics from cycloolefins. Benzene is converted to cyclohexylbenzene by acid catalyzed alkylation with cyclohexene. 1 vinyl 3 cyclohexene dioxide reacts with active hydrogen compounds such as alcohols and amines.

Compounds in this group react with acids bases and oxidizing and reducing agents. These polymerization reactions can be violent. Enev4520 2 8 p273 avoid release to the environment p303 p361 p353 if on skin or hair. Cyclohexylbenzene is a precursor to both phenol and cyclohexanone.

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.