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Urazole, 4-amino

Triazole has been prepared by the oxidation of substituted 1,2,4-triazoles, by the treatment of urazole with phosphorus pentasulfide, by heating equimolar quantities of formyl-hydrazine and formamide, by removal of the amino function of 4-amino-l,2,4-triazole, by oxidation of l,2,4-triazole-3(5)-thiol with hydrogen peroxide, by decarboxylation of 1,2,4-triazole-3(5)-carboxylic acid, by heating hydrazine salts with form-amide,by rapidly distilling hydrazine hydrate mixed with two molar equivalents of formamide, i by heating N,N -diformyl-hydrazine with excess ammonia in an autoclave at 200° for 24 hours, and by the reaction of 1,3,5-triazine and hydrazine monohydrochloride. ... [Pg.102]

This structure was assigned by Curtius Heidenreich to the compd described in Vol 1, p A472-L as 4-Amino urazole Refs Same as given in Vol 1, p A472-L... [Pg.417]

An irio-3-cxy- 1,2,4 fnazole [Called m Bti 5-Oxo-3-imino-1.2.4-triazolidin, Urazol-monoimid. 5-Amino-1.2.4-triazolon-(3) or Imidurazoll (Called in JCS I minourazole),... [Pg.240]

Diurea. See in Vol 1, A472-L under 4-Amino-Urazole and in Vol 5, D1523-L... [Pg.127]

N itros amino urazole, C3H3N303 and Nitrami-nourazole, Ca H3NS O, — not found in Beil or CA through 1956... [Pg.272]

N3C2H202(NH2) Urazine (4-amino-urazole), 4 29 salts, 4 31 NsCs Cesium azide, 1 79 NSH Hydrazoic acid, 1 77, 78 Hydrogen azide, 1 77, 78 N3K Potassium azide, 1 79 2 139, 140... [Pg.213]


See other pages where Urazole, 4-amino is mentioned: [Pg.920]    [Pg.494]    [Pg.558]    [Pg.588]    [Pg.920]    [Pg.173]    [Pg.210]    [Pg.233]    [Pg.417]    [Pg.433]    [Pg.920]    [Pg.920]    [Pg.193]    [Pg.633]   
See also in sourсe #XX -- [ Pg.53 , Pg.132 ]




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