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ARENEDIAZO ARYL SULFIDES

Acyl or alkyl nitrates Alkyl perchlorates Aminemetal oxosalts Arenediazo aryl sulfides Arenediazoniiimolates Azo compounds... [Pg.2313]

See also ALKANETHIOLS, ALKENEBIS(SULFONIUM PERCHLORATES) allyl trifluo-ROMETHANESULFONATES, ARENEDIAZO ARYL SULFIDES BIS(ARENEDIAZO) sulfides, BIS(SULFURDIIMIDES DIAZONIUM SULFATES, DIAZONIUM SULFIDES AND DERIVATIVES METAL AMIDOSULFATES, METAL PHOSPHORUS TRISULFIDES METAL SULFATES, METAL SULFIDES, NON-METAL SULFIDES SULFONIC ACID ESTERS, SULFUR BLACK, SULFUR ESTERS THIOPHENOXIDES, XANTHATES ... [Pg.396]

Interaction of 2-, 3- or 4-chlorobenzenediazonium salts with (9-alkyldithiocarbon-ate ( xanthate ) solutions [8] or thiophenoxide solutions [9] produces explosive products, possibly arenediazo aryl sulfides. The intermediate diazonium xanthate produced during the preparation of m-thiocresol can be dangerously explosive under the wrong conditions [8], while the reaction of 3-nitrobenzenediazonium chloride with xanthate solution at 70—75°C proceeds with near-explosive evolution of nitrogen [4]. The product of interaction of 2-chlorobenzenediazonium chloride and sodium 2-chlorothiophenoxide exploded violently on heating to 100°C, and the oil... [Pg.2304]

Arenecyclopentadienyliron(ii) picrates, 44 Arenediazo aryl sulfides, 44 Arenediazoates, 44 Arenediazonium oxides, 44 Artificial fingernails, 45 Aryl chloroformates, 45 2-Arylideneamino-4,6-dinitrophenol salts, 45 Arylmetals, 45... [Pg.2636]

See other pages where ARENEDIAZO ARYL SULFIDES is mentioned: [Pg.31]    [Pg.62]    [Pg.118]    [Pg.43]    [Pg.99]    [Pg.2248]    [Pg.2166]    [Pg.31]    [Pg.62]    [Pg.118]    [Pg.43]    [Pg.99]    [Pg.2248]    [Pg.2166]    [Pg.457]   
See also in sourсe #XX -- [ Pg.44 ]



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Aryl sulfides

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