125 at lower temperatures optically active 4 exo dideuteriovinyl cyclohexene undergoes both racemization and deuterium scrambling to c 3.
Vinyl cyclohexene 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.
It is soluble in water.
10 17 2016 en english us sds id.
Epoxides are highly reactive.
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.
126 these processes occur with log k rac 12 09 49 650 2 3rt and.
However it slowly hydrolyzes in aqueous solutions akron 2009.
They polymerize in the presence of catalysts or when heated.
Physical and chemical properties of 4 vinyl 1 cyclohexene diepoxide are listed in the following table.
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The main 4 vinyl 1 cyclohexene metabolite formed in mice liver microsomes after incubation was 4 vinylcyclohexane 1 2 diol.
Compounds in this group react with acids bases and oxidizing and reducing agents.
Journal of analytical and applied pyrolysis 1988 13 4 259 275.
4 vinyl 1 cyclohexene safety data sheet print date.
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.
4 vinylcyclohexene is an organic compound consisting of a vinyl group attached to the 4 position of the cyclohexene ring.
Cyclohexylbenzene is a precursor to both phenol and cyclohexanone.
These polymerization reactions can be violent.
Properties 4 vinyl 1 cyclohexene diepoxide is a colorless liquid at room temper ature ntp 1989.
4 vinyl 1 cyclohexene dioxide increased approx 10 times the forward mutation rate of v79 chinese hamster cells.
Take off immediately all contaminated clothing.
Conditions to avoid excess heat.
Enev4520 2 8 p273 avoid release to the environment p303 p361 p353 if on skin or hair.
Other metabolites were 4 vinyl 1 2 epoxycyclohexane 4 vinyl 1 cyclohexene dioxide.
Although chiral it is used mainly as the racemate.
It is a colorless liquid.
It is a precursor to vinylcyclohexene dioxide.
Benzene is converted to cyclohexylbenzene by acid catalyzed alkylation with cyclohexene.
