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Difluoroamino compounds

However, when the addition is performed 111 a nucleopliilic solvent such as methanol, cleavage of the imine linkage occurs to give difliioroamino compounds [78] (equation 12) W, At-Difluorotrifluoromethylamine can be prepared from or from thiocyanates, as shown in equation 13 [79, 80] Another way to produce difluoroamino compounds is the addition of fluorine to nitriles by means of AgFj [Sf ] or C0F3 [S/]... [Pg.45]

Uses. Its primary use is in the prepn of organic difluoroamino compounds, A 1 1 adduct of difluoramine with methyl ether can be used as a rocket proplnt, Isp 229sec at lOOOpsia. In... [Pg.307]

Poly (Difluoroamino)-Substituted Cyanuric and Isocyanuric Acid Derivatives. For Cyanuric Acid and Derivatives see Vol 3, C589-R ff. For Difluoroamino Compounds see Vol 5, DI258-L... [Pg.811]

Perfluoro-iV-cyanodiaminomethane [16408-94-9] F2NCF2N(F)C=N See Fluorine Sodium dicyanamide See Other CYANO COMPOUNDS, DIFLUOROAMINO COMPOUNDS c2f5n3... [Pg.247]

See other catalytic impurity incidents, difluoroamino compounds, /v-nitro... [Pg.304]

Samples of this and related poly-difluoroamino compounds exploded during analytical combustion. [Pg.613]

Many compounds containing one or more N—X bonds show unstable or explosive properties (and are also oxidants), and this topic has been reviewed [1]. Difluoroamino compounds, ranging from difluoramine and tettafluorohydrazine to polydifluoroamino compounds, are notably explosive and suitable precautions have been detailed [2,3], Preparative scale A-chlorination of ly and 2y amines by passing them over N-chlorosuccinimide is described. In presence of alumina, ly amines give the N,N -dichloro derivatives. The products must be handled with... [Pg.182]

N -CHLORONITROAMINES DIFLUOROAMINO COMPOUNDS HALOGEN AZIDES N -HALOIMIDES... [Pg.183]

CYCLIC PEROXIDES, DIACYL PEROXIDES DIALKYL PEROXIDES, Z, /-DI(BENZOYLPEROXY)ARYLIODINES DIFLUOROAMINO COMPOUNDS, DIFLUOROAMINOPOLYNITROAROMATIC COMPOUNDS... [Pg.306]

This group of compounds, (which combines the structural features of both the separately treated A+haloimides and difluoroamino compounds, each of high reactivity) is explosively unstable. [Pg.411]

See Acetonitrile A-Fluoro compounds See other DIFLUOROAMINO COMPOUNDS... [Pg.156]


See other pages where Difluoroamino compounds is mentioned: [Pg.237]    [Pg.161]    [Pg.237]    [Pg.168]    [Pg.143]    [Pg.145]    [Pg.145]    [Pg.146]    [Pg.146]    [Pg.147]    [Pg.161]    [Pg.246]    [Pg.250]    [Pg.304]    [Pg.401]    [Pg.488]    [Pg.507]    [Pg.508]    [Pg.613]    [Pg.1534]    [Pg.1535]    [Pg.75]    [Pg.125]    [Pg.125]    [Pg.125]    [Pg.150]    [Pg.56]    [Pg.106]    [Pg.106]    [Pg.106]    [Pg.131]    [Pg.24]    [Pg.423]   
See also in sourсe #XX -- [ Pg.5 ]

See also in sourсe #XX -- [ Pg.107 ]




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