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Carbonyl dicyanide

Oxopropanedinitrile (Carbonyl dicyanide) [1115-12-4] 0 C(CN)2 Water Martin, E. L., Org. Synth., 1971, 51, 70 The nitrile reacts explosively with water. See related ACYL HALIDES See other CYANO COMPOUNDS c3n2o... [Pg.470]

Carbonyl-bis(triphenylphosphine)iridium—silver diperchlorate, 3892 Carbonyl dicyanide, see Oxopropanedinitrile, 1337 Carbonyl difluoride, 0342a Carbonyl diisothiocyanate, 1338 Carbonyl(pentasulfur pentanitrido)molybdenum, 0532 2-Carboxy-3,6-dimethylbenzenediazonium chloride, 3132a Carboxymethyl carbamimoniothioate chloride,... [Pg.2062]

Phosgene can be used as the starting material for the preparation of other potentially useful carbonyl halides and carbonyl pseudohalides. Reaction of phosgene with fluorspar, for example, gives COCIF (see Section 9.1.1 and Chapter 16). With aluminium(III) bromide, COBrj is formed (Section 9.1.2.6). Reaction of COClj with HF gives COFj (see Section 9.10.4 and Chapter 13), reaction with silver cyanide gives carbonyl dicyanide, CO(CN)j (Section 9.1.7), whereas reaction with a mixture of sodium fluoride and HCN gives the mixed carbonyl halide pseudohalide, COFCN (Section 9.1.7 and Chapter 13). The chemistry of these... [Pg.216]

With KCN, however, no carbonyl dicyanide was produced [ICI30] ... [Pg.356]

The nitrile, MejSiCN, interacts with COClj to give carbonyl dicyanide, CO(CN)j, which reacts with a further molecule of MCgSiCN to form Mc3SiOC(CN)3 [1250] ... [Pg.496]

Carbonyl chloride fluoride Carbonyl dicyanide W./i/ -Carbonyldiimidazole Carbonyl fluoride... [Pg.190]


See other pages where Carbonyl dicyanide is mentioned: [Pg.529]    [Pg.418]    [Pg.534]    [Pg.463]    [Pg.1975]    [Pg.211]    [Pg.987]    [Pg.1385]    [Pg.203]    [Pg.973]    [Pg.1331]    [Pg.1051]    [Pg.550]    [Pg.942]    [Pg.235]    [Pg.236]    [Pg.1189]    [Pg.1551]    [Pg.1064]    [Pg.223]    [Pg.224]    [Pg.1099]    [Pg.1497]    [Pg.234]    [Pg.235]    [Pg.1186]    [Pg.1551]    [Pg.971]    [Pg.1329]   
See also in sourсe #XX -- [ Pg.356 , Pg.416 , Pg.533 ]




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