Diazole- and triazole-4,5-dicarboxylic acids and their derivatives. Synthesis was written by Stepanyan, A. A.;Isak, A. D.. And the article was included in Khimichna Promislovist Ukraini (Kiev, Ukraine) in 2008.COA of Formula: C4H3N3O4 This article mentions the following:
Oxidation of indazole, benzotriazole, 1-methylbenzimidazole and 2-methylbenzimidazole by ozone gave 4,5-pyrazoledicarboxylic acid, 1,2,3-triazole-4,5-dicarboxylic acid, 1-methyl-4,5-imidazoledicarboxylic acid and 2-methyl-4,5-imidazoledicarboxylic acid, resp. In the experiment, the researchers used many compounds, for example, 1H-1,2,3-Triazole-4,5-dicarboxylic acid (cas: 4546-95-6COA of Formula: C4H3N3O4).
1H-1,2,3-Triazole-4,5-dicarboxylic acid (cas: 4546-95-6) belongs to triazole derivatives. Triazoles consist of a five-membered ring containing three nitrogen atoms and are biologically active, especially as antifungal, antimicrobial and enzyme inhibitors. Many triazoles have antifungal effects: the triazole antifungal drugs include fluconazole, isavuconazole, itraconazole, voriconazole, pramiconazole, ravuconazole, and posaconazole and triazole plant-protection fungicides include epoxiconazole, triadimenol, myclobutanil, propiconazole, prothioconazole, metconazole, cyproconazole, tebuconazole, flusilazole and paclobutrazol.COA of Formula: C4H3N3O4
Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics