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SYNTHESIS OF N-(1-METHYLTETRAZOL-5-YL)TRINITROACETIMIDAMIDE

Владимир А. Заломленков, Владимир В. Бахарев, Александр А. Гидаспов, Виктор Е. Парфенов, Ольга В. Головина, Павел А. Слепухин
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Abstract


The reaction of 3-methyl-5-trinitromethyltetrazolо[1,5-а][1,3,5]triazin-7-one with water led to the opening of 1,3,5-triazine ring and preservation of trinitromethyl group in the product. The obtained N-(1-methyltetrazol-5-yl)trinitroacetimidamide is of interest as high-energy compound.

Authors: Vladimir A. Zalomlenkov, Vladimir V. Bakharev*, Alexander A. Gidaspov, Victor E. Parfenov, Olga V. Golovina, Pavel A. Slepukhin


Keywords


tetrazolо[1,5-а][1,3,5]triazine; tetrazolyltrinitroacetimidamide; trinitromethyl-1,3,5-triazine; hydrolysis; ring opening

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Latvian Institute of Organic Synthesis - Aizkraukles iela, 21, Riga, LV-1006, Latvia - hgs@osi.lv