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Nitroguanyl azide

The substance (II) is converted by the action of nitrous acid into nitroguanyl azide (Ha) at 0°C or into nitraminotetrazole (lib) (Lieber et al. [53]) at 70°C. Both substances are explosive ... [Pg.28]

In some special cases the azides could be isolated. One example is the stable nitroguanyl azide (286), which served for the synthesis of 5-nitrairiinotetrazole (287)... [Pg.383]

See other pages where Nitroguanyl azide is mentioned: [Pg.636] [Pg.211] [Pg.261] [Pg.211] [Pg.261] [Pg.211] [Pg.261] [Pg.211] [Pg.261] [Pg.513] [Pg.514] [Pg.211] [Pg.261] [Pg.400] [Pg.636] [Pg.211] [Pg.261] [Pg.211] [Pg.261] [Pg.211] [Pg.261] [Pg.211] [Pg.261] [Pg.513] [Pg.514] [Pg.211] [Pg.261] [Pg.400]

See also in sourсe #XX -- [ Pg.28 ]

See also in sourсe #XX -- [ Pg.400 ]