Compounds in this group react with acids bases and oxidizing and reducing agents.
Vinyl cyclohexene reaction.
It is a precursor to vinylcyclohexene dioxide.
10 17 2016 en english us sds id.
Conditions to avoid excess heat.
It is produced by 1 3 butadiene dimerizes in a diels alder reaction.
It is a colorless liquid.
125 at lower temperatures optically active 4 exo dideuteriovinyl cyclohexene undergoes both racemization and deuterium scrambling to c 3.
1 vinyl 3 cyclohexene dioxide reacts with active hydrogen compounds such as alcohols and amines.
However it slowly hydrolyzes in aqueous solutions akron 2009.
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.
4 vinyl 1 cyclohexene dioxide increased approx 10 times the forward mutation rate of v79 chinese hamster cells.
Properties 4 vinyl 1 cyclohexene diepoxide is a colorless liquid at room temper ature ntp 1989.
Although chiral it is used mainly as the racemate.
Other metabolites were 4 vinyl 1 2 epoxycyclohexane 4 vinyl 1 cyclohexene dioxide.
These polymerization reactions can be violent.
Journal of analytical and applied pyrolysis 1988 13 4 259 275.
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.
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.
Cyclohexylbenzene is a precursor to both phenol and cyclohexanone.
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The main 4 vinyl 1 cyclohexene metabolite formed in mice liver microsomes after incubation was 4 vinylcyclohexane 1 2 diol.
Epoxides are highly reactive.
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.
Take off immediately all contaminated clothing.
Rearrangement reactions in the thermal formation of aromatics from cycloolefins.
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.
Benzene is converted to cyclohexylbenzene by acid catalyzed alkylation with cyclohexene.
