N-HALOGEN COMPOUNDS

A,V,V-trifliioroalkylamidines N-halogen compounds N-metal derivatives Nitroalkanes, c-nitro, and polynitroaryl compounds... 

Decomposition is explosive at 155°C, and accelerated by contact with metals. See other azo compounds, n-halogen compounds... 

See other endothermic compounds, n-halogen compounds, oxidants... 

C,N-Pcrlluoro-A -aminomethyltriaminomethane, 0649 Pcrlluoro-A -cyanodiaminomethane, 0637 f Tetrafluorohydrazine, 4345 Tctrail uorourca, 0352 Tris(difluoroamino)lluoromethane, 0364 See BIS(DIFLUOROAMINO)ALKYL NITRATES See other N-HALOGEN COMPOUNDS... 

Tris(thionitrosyl)thallium, 4764 See also N -HALOGEN COMPOUNDS... 

As it is potentially explosive in neat liquid or solid forms, it is best handled in solution. See other DIAZIRINFS, N-HALOGEN COMPOUNDS... 

See entry N-HALOGEN COMPOUNDS (reference 4) See other AT.T.YT. COMPOUNDS... 

After refluxing for 24 hours at 105°C, a mixture exploded, possibly due to dehydro-halogenation of the bromonitrile to acrylonitrile, and polymerisation of the latter. See Other N-HALOGEN COMPOUNDS, /V-HAI.OIMIDES... 

A sample exploded on vacuum distillation at 60°C, though not at 40°C/33 mbar. See Other N-HALOGEN COMPOUNDS, N—NITRO COMPOUNDS... 

It explodes on heating, like the bis-chloroimine. See other N-HALOGEN COMPOUNDS... 

See other DIAZIRINES, N-HALOGEN COMPOUNDS, NITROARYL COMPOUNDS... 

Gallacher, T. C. et al., J. Chem. Soc., Chem. Comm., 1979, 420 Thermal decomposition is vigorous, and was explosive on one occasion. See other N-HALOGEN COMPOUNDS, TETRAZOLES... 

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