Anderson, David J. et al. published their research in Journal of the Chemical Society in 1973 | CAS: 4546-95-6

1H-1,2,3-Triazole-4,5-dicarboxylic acid (cas: 4546-95-6) belongs to triazole derivatives. Many triazoles are versatile, biologically active compounds commonly used as fungicides and plant retardants.Triazole heterocyclic structures are found to form many weak nonbond interactions with the receptors and enzymes in biological systems.Related Products of 4546-95-6

Reactive intermediates. XXII. Formation of 2H-azirines by oxidation of N-aminophthalimide in the presence of alkynes was written by Anderson, David J.;Gilchrist, Thomas L.;Gymer, Geoffrey E.;Rees, Charles W.. And the article was included in Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999) in 1973.Related Products of 4546-95-6 This article mentions the following:

Pb(OAc)4 oxidation of N-aminophthalimide in the presence of HCCMe gave 1% 3-methyl-2-phthalimido-2H-azirine (I); HCCPr, MeCCMe, and EtCCEt formed 5-15% of analogous azirines. 1,2,3-Triazole-4,5-dicarboxylic acid with Ac2O gave 2-methyloxazole-4-carboxylic acid. In the experiment, the researchers used many compounds, for example, 1H-1,2,3-Triazole-4,5-dicarboxylic acid (cas: 4546-95-6Related Products of 4546-95-6).

1H-1,2,3-Triazole-4,5-dicarboxylic acid (cas: 4546-95-6) belongs to triazole derivatives. Many triazoles are versatile, biologically active compounds commonly used as fungicides and plant retardants.Triazole heterocyclic structures are found to form many weak nonbond interactions with the receptors and enzymes in biological systems.Related Products of 4546-95-6

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics