Benzene is converted to cyclohexylbenzene by acid catalyzed alkylation with cyclohexene.
Vinyl cyclohexene reaction.
Journal of analytical and applied pyrolysis 1988 13 4 259 275.
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Cyclohexene is produced by the partial hydrogenation of benzene a process developed by the asahi chemical company.
4 vinylcyclohexene is an organic compound consisting of a vinyl group attached to the 4 position of the cyclohexene ring.
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.
Stability and reactivity reactive hazard none known based on information available stability stable under normal conditions.
However it slowly hydrolyzes in aqueous solutions akron 2009.
They polymerize in the presence of catalysts or when heated.
Enev4520 2 8 p273 avoid release to the environment p303 p361 p353 if on skin or hair.
Take off immediately all contaminated clothing.
10 17 2016 en english us sds id.
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.
Compounds in this group react with acids bases and oxidizing and reducing agents.
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.
It is a precursor to vinylcyclohexene dioxide.
Epoxides are highly reactive.
These polymerization reactions can be violent.
It is soluble in water.
125 at lower temperatures optically active 4 exo dideuteriovinyl cyclohexene undergoes both racemization and deuterium scrambling to c 3.
Although chiral it is used mainly as the racemate.
The main 4 vinyl 1 cyclohexene metabolite formed in mice liver microsomes after incubation was 4 vinylcyclohexane 1 2 diol.
Physical and chemical properties of 4 vinyl 1 cyclohexene diepoxide are listed in the following table.
Conditions to avoid excess heat.
4 vinyl 1 cyclohexene safety data sheet print date.
Properties 4 vinyl 1 cyclohexene diepoxide is a colorless liquid at room temper ature ntp 1989.
Rearrangement reactions in the thermal formation of aromatics from cycloolefins.
4 vinyl 1 cyclohexene dioxide increased approx 10 times the forward mutation rate of v79 chinese hamster cells.
