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Metazonic acid

When the nitrile-oxide is treated with 5 % aqueous NaOH at 0° C, three products can be isolated the two isomers XXXIV and XXXV and the metazonic acid XXXVI the latter, on heating in boiling xylene is transformed into XXXIV (66, 68, 78). [Pg.176]

It is produced by the action of sodium hydroxide on nitromethane at an elevated temperature (Friese [72] Steinkopf and Kirchhoff [73]). Urbanski and Kowalczyk [74] found that some heavy metal salts of this compound have weak initiating properties and that metazonic acid itself is a fairly weak explosive. Its expansion in the lead block is 240 cm3. [Pg.224]

A convenient preparative method for the synthesis of 2-substituted 4-nitro-l,2,3-triazoles is based on the condensation of diazonium salts with metazonic acid. The latter is in turn synthesized by the action of alkali on nitromethane [423,508-510] (Scheme 78). [Pg.45]

Other slyphnates Lead dinitroresorcinale Nitrosophcnol salts Nitraminc salts Salts of metazonic acid Salts of oxalic acid Peroxides... [Pg.348]


See other pages where Metazonic acid is mentioned: [Pg.224]    [Pg.224]    [Pg.224]    [Pg.224]   
See also in sourсe #XX -- [ Pg.224 ]




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Metazonic acid salts

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