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Ethylene bromide chlorohydrin

CROTONALDEHYDE CYCLOHEXAN(X CYCLOHEXANONE DIMETHYLAMINE DIOCTYLPHTHALATE ESTERS ETHERS ETHYL ACETATE ETHYL ACRYLATE ETHYL CHLORIDE ETHYL ETHER ETHYLENE BROMIDE ETHYLENE CHLOROHYDRIN... [Pg.154]

The manufacture of a related compound is first described. 28.1 parts of p-chloro-benzhy-dryl bromide are heated to boiling, under reflux and with stirring, with 50 parts of ethylene chlorohydrin and 5.3 parts of calcined sodium carbonate. The reaction product is extracted with ether and the ethereal solution washed with water and dilute hydrochloric acid. The residue from the solution in ether boils at 134° to 137°C under 0.2 mm pressure and is p-chloro-benzhydryl-(/3-chloroethyl) ether. [Pg.375]

C3H4O3 96-49-1) see Hexcarbacholine bromide Raloxifene hydrochloride ethylene chlorohydrin... [Pg.2379]

Ethylene chlorohydrin, 30, 11 33, 11 Ethylene dibromide, 30, 35 Ethylene diisothiuronium bromide, 30, 36... [Pg.55]

Ethyl bromide, I, i, 6-7 Ethyl 8-bromopropionate, HI, 51-52 Ethyl cyanoacetate. III, 53-56 Ethylene chlorohydrin, 111, 7 Ethyl ether. III, 47, 48 Ethyl hydracrylate. III, 52 Ethyl oxalate, II, 23-26 Ethyl phenylacetate, II, 27-28 Extraction, III, 88... [Pg.52]

METHYL-, HYDROCHLORIDE, 31, 37 Ethyl benzoylacetate, 32, 85 O-Ethylcaprolactim, 31, 73 Ethyl chloroacetate, 30, 7 Ethyl 0-chloroisocrotonate, 32, 78 Ethyl cyanoacetate, 32, 45 Ethyl dichloroacetate, 32, 47 Ethylene, 32, 100 Ethylene, tetraphenyl-, 31, 104 Ethylene chlorohydrin, 30, 11 Ethylene dibromide, 30, 35 Ethylene diisothiuronium bromide, 30, 36... [Pg.58]

ETHYL BENZENE ETHYL BROMIDE ETHYL CHLORIDE ETHYL ETHER ETHYLENE CHLOROHYDRIN ETHYLENE DIAMINE ETHYLENE DIBROMIDE ETHYLENE DICHLORIDE ETHYLENE GLYCOL ETHYLENEIMINE ETHYLENE OXIDE DIETHYL KETONE DIETHYLENE GLYCOL GLYCOL ETHERS, ESTERS MEA, DEA. TEA VINYL ACETATE POLYMERS. COPOLYMERS... [Pg.518]

Phenylethyl alcohol is prepared by reduction of ethyl phenyl-acetate with sodium in absolute alcohol by hydrogenation of phenylacetaldehyde in the presence of a nickel catalyst or by addition of ethylene oxide or ethylene chlorohydrin to phenylmagnesium bromide, followed by hydrolysis. Phenylethyl alcohol also occurs naturally in a number of essential oils, especially rose oil. [Pg.520]


See other pages where Ethylene bromide chlorohydrin is mentioned: [Pg.134]    [Pg.68]    [Pg.51]    [Pg.1680]    [Pg.924]    [Pg.165]    [Pg.375]    [Pg.303]    [Pg.53]    [Pg.1489]    [Pg.1498]    [Pg.66]    [Pg.589]    [Pg.1103]    [Pg.786]    [Pg.461]    [Pg.1540]    [Pg.375]    [Pg.138]   
See also in sourсe #XX -- [ Pg.190 ]




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Chlorohydrination

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Ethylene bromide

Ethylene chlorohydrin

Ethylene chlorohydrination

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