Vinyl Cyclohexane Cas

Beilstein reaxys number 1901553.

Vinyl cyclohexane cas.

The reaction is conducted at 110 425 c at pressures of 1 3. 4 ethenyl 1 cyclohexene nsc 15760 cas number 100 40 3. 2 h315 eye irrit. 4 vinyl 1 cyclohexene cas no.

2 h225 skin irrit. Linear formula c 6 h 9 ch ch 2. It is produced by 1 3 butadiene dimerizes in a diels alder reaction. 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.

Find sigma aldrich 677388 msds related peer reviewed papers technical documents similar products more at sigma aldrich. The main 4 vinyl 1 cyclohexene metabolite formed in mice liver microsomes after incubation was 4 vinylcyclohexane 1 2 diol. Other metabolites were 4 vinyl 1 2 epoxycyclohexane 4 vinyl 1 cyclohexene dioxide. 100 40 3 name product identifier ghs us classification 4 vinyl 1 cyclohexene cas no 100 40 3 97 100 flam.

It is a colorless liquid. Molecular weight 108 18. Although chiral it is used mainly as the racemate. Vinyl cyclohexane diepoxide chemical information properties structures articles patents and more chemical data.

Pubchem substance id 329829033. 4 vinyl 1 cyclohexene dioxide increased approx 10 times the forward mutation rate of v79 chinese hamster cells. It is a precursor to vinylcyclohexene dioxide. 1 4 cyclohexane dimethanol divinyl ether is a versatile vinyl monomer that offers unique application properties.

4 vinylcyclohexene is an organic compound consisting of a vinyl group attached to the 4 position of the cyclohexene ring. Enter your search term above and find. 2 h361 aquatic acute 2 h401 2 6 di tert.