Vinyl cyclohexane diepoxide chemical information properties structures articles patents and more chemical data.
Vinyl cyclohexane cas.
It is produced by 1 3 butadiene dimerizes in a diels alder reaction.
Linear formula c 6 h 9 ch ch 2.
It is a precursor to vinylcyclohexene dioxide.
Obtained by hydrogenation of poly styrene.
Although chiral it is used mainly as the racemate.
1 4 cyclohexane dimethanol divinyl ether is a versatile vinyl monomer that offers unique application properties.
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The reaction is conducted at 110 425 c at pressures of 1 3.
2 h225 skin irrit.
Poly vinyl cyclohexane cas number.
Molecular weight 108 18.
2 h361 aquatic acute 2 h401 2 6 di tert.
100 40 3 name product identifier ghs us classification 4 vinyl 1 cyclohexene cas no 100 40 3 97 100 flam.
Beilstein reaxys number 1901553.
Very low viscosity of 4 mpas at room temperature high cure speed in cationic curing formulations excellent reactive diluent with the film properties of a binder cures to coatings with high impact strength1 4 cyclohexane dimethanol divinyl ether can be used in multiple applications.
Pubchem substance id 329829033.
4 vinyl 1 cyclohexene dioxide increased approx 10 times the forward mutation rate of v79 chinese hamster cells.
4 vinyl 1 cyclohexene cas no.
The main 4 vinyl 1 cyclohexene metabolite formed in mice liver microsomes after incubation was 4 vinylcyclohexane 1 2 diol.
4 ethenyl 1 cyclohexene nsc 15760 cas number 100 40 3.
It is a colorless liquid.
2 h315 eye irrit.
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