Ring-chain tautomeric transformations of the product of diazotization of 5-(2′-aminophenyl)tetrazole
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Abstract
It was established on the basis of IR spectral data that the products of the reaction of 5-(2′-aminophenyl)tetrazole and 4-hydrazinobenzo-1,2,3-triazine with amyl nitrite have the 5-(2′-diazoniaphenyl)tetrazolestructure in the crystalline state. A study of the UV spectra of the latter showed that in methanol solution it exists in equilibrium with the isomeric 4-azidobenzo-1,2,3-triazine.
Keywords
Methanol Organic Chemistry Nitrite Spectral Data Tetrazole
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© Plenum Publishing Corporation 1982