Methyl Vinyl Ether

34 6 deg and other impurities.

Methyl vinyl ether.

It is soluble in water use. 35 5 deg is accompanied by diethyl ether b p. The vinyl carbonate 13 152 gives only copolymerization the ketene acetal 11 153 and the methyl vinyl ether 14 152 give both copolymerization and chain transfer in styrene polymerization whereas with the benzyl vinyl ethers 12 153 15 8 and 16 18 151 chain transfer is the only reaction detected. In general vinyl ethers possessing highly branched alkyl groups are more reactive than those bearing straight chain alkyl groups.

The reactivity of the vinyl ethers in cationic polymerization depends on both the initiator used and the structure of the vinyl ether itself. Vinyl methyl ether is a colorless gas. Workers that produce or use vinyl methyl ether may breathe in mists or have direct skin contact. It is used as a synthetic building block and a monomer.

Vinyl methyl ether reacts vigorously with oxidizing materials. Structure properties spectra suppliers and links for. The synthesized vinyl ethyl ether b p. Using a relative kinetic method rate coefficients in units of cm3 molecule 1 s 1 of 7.

Ethyl vinyl ether is an organic compound with the chemical formula ch 3 ch 2 och ch 2. Linear formula ch 3 och ch 2. Methyl vinyl ether 98 synonym. A satisfactory separation has been made by gas chromatography in a 2 m dimethylsulfolane column followed by a 3 m squalane column on celite.

Beilstein reaxys number 1209255. Reacts possibly explosively with halogens bromine chlorine or hydrogen halides hydrogen bromide hydrogen chloride baker 1980 p. Methyl vinyl ether 107 25 5. Explosive in the form of vapor when exposed to heat flame or strong oxidizing agents.

Methoxyethylene cas number 107 25 5. It is the simplest enol ether that is liquid at room temperature. Molecular weight 58 08.