Although chiral it is used mainly as the racemate.
Vinyl cyclohexene reaction.
These polymerization reactions can be violent.
However it slowly hydrolyzes in aqueous solutions akron 2009.
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.
126 these processes occur with log k rac 12 09 49 650 2 3rt and.
10 17 2016 en english us sds id.
Properties 4 vinyl 1 cyclohexene diepoxide is a colorless liquid at room temper ature ntp 1989.
Cyclohexylbenzene is a precursor to both phenol and cyclohexanone.
Physical and chemical properties of 4 vinyl 1 cyclohexene diepoxide are listed in the following table.
4 vinyl 1 cyclohexene dioxide increased approx 10 times the forward mutation rate of v79 chinese hamster cells.
It is produced by 1 3 butadiene dimerizes in a diels alder reaction.
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.
Stability and reactivity reactive hazard none known based on information available stability stable under normal conditions.
Cyclohexene is produced by the partial hydrogenation of benzene a process developed by the asahi chemical company.
Conditions to avoid excess heat.
It is a colorless liquid.
125 at lower temperatures optically active 4 exo dideuteriovinyl cyclohexene undergoes both racemization and deuterium scrambling to c 3.
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.
1 vinyl 3 cyclohexene dioxide reacts with active hydrogen compounds such as alcohols and amines.
Take off immediately all contaminated clothing.
Benzene is converted to cyclohexylbenzene by acid catalyzed alkylation with cyclohexene.
Epoxides are highly reactive.
4 vinyl 1 cyclohexene safety data sheet print date.
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The main 4 vinyl 1 cyclohexene metabolite formed in mice liver microsomes after incubation was 4 vinylcyclohexane 1 2 diol.
They polymerize in the presence of catalysts or when heated.
It is soluble in water.
Enev4520 2 8 p273 avoid release to the environment p303 p361 p353 if on skin or hair.
Compounds in this group react with acids bases and oxidizing and reducing agents.
