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Thiocarbamic 0-aryl esters

Carbamate compounds are usually subdivided into at least three main groups with respect to their structure and general use (see Figure 1) insecticides, herbicides, and thio- or dithiocarbamates. A variety of R groups may be substituted in the molecule producing, as is the case for insecticides, a variety of alkyl or aryl esters of carbamic acid. Although technically characterized as carbamate pesticides, thio- and di-thiocarbamate fungicides are not included in this... [Pg.410]

Aryl TV-substituted thiocarbamates 787 An 0-aryl chlorothioformate (1 mole) is dropped slowly into a solution of an amine (2 moles) in acetone or ethanol at 20-30°, with stirring. After a further hour s stirring, the mixture is poured into water, and the precipitated ester is collected, dried, and recrystallized from ethanol. [Pg.689]


See other pages where Thiocarbamic 0-aryl esters is mentioned: [Pg.2243]    [Pg.2243]    [Pg.2439]    [Pg.164]    [Pg.1512]    [Pg.166]    [Pg.588]    [Pg.2159]    [Pg.1043]    [Pg.366]    [Pg.198]   
See also in sourсe #XX -- [ Pg.689 ]




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Aryl esters

Esters arylation

Esters thiocarbamic

Thiocarbamate

Thiocarbamates

Thiocarbamates Thiocarbamic esters

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