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Chloroethyl chlorosulphonate

Also halogenated derivatives of ethyl chlorosulphonate Chloroethyl Chlorosulphonate... [Pg.255]

It also reacts with ethylene chlorohydrin, forming chloroethyl chlorosulphonate ... [Pg.260]

In class B are placed all simple esters, CHjF CO i , of fluoro-aoetic acid, where iZ = Me, Et, Pr , Pr , Ph, etc. When substitution takes place in the a-hydrogen atoms, e.g. in methyl a-fluoropropionate or a-fluoroisobutyrate, then the compound is devoid of toxicity. This indicates the importance of the unsubstituted fluoromethyl group. On pp. 125 et seq. it was shown that fluoroacetamide and a variety of substituted amides such as CHjF CO NH CHg CHjCl were, molecule for molecule, equally toxic with fluoroacetic acid and produced the same symptoms. The 2 chloroethyl group therefore contributed nothing appreciable to the toxicity of the molecule. The majority of the esters of fluoroethanol showed the toxicity of the parent alcohol, e.g. 2-fluoroethyl chlorosulphonate, CHgF CHg O SOjCl, di-(2-fluoroethyl) sulphate and 2-fluoroethylglycine hydrochloride. [Pg.134]


See other pages where Chloroethyl chlorosulphonate is mentioned: [Pg.147]    [Pg.134]   
See also in sourсe #XX -- [ Pg.255 , Pg.260 ]




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Chlorosulphonated

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