Ionic strength dependence of formation constants. Part 20. Salt effects on the protonation of 1H-1,2,3-trazole-4,5-dicarboxylic acid in aqueous solution was written by De Robertis, Alessandro;Foti, Claudia;Gianguzza, Antonio. And the article was included in Journal of Chemical Research, Synopses in 1995.Synthetic Route of C4H3N3O4 This article mentions the following:
The dependence on ionic strength of the protonation constants of 1H-1,2,3-triazole-4,5-dicarboxylic acid has been studied in Et4NI, NaCl and CaCl2 aqueous solution, and it has been found that the complexation behavior of this ligand is very similar to that of tricarboxylic acids. In the experiment, the researchers used many compounds, for example, 1H-1,2,3-Triazole-4,5-dicarboxylic acid (cas: 4546-95-6Synthetic Route of C4H3N3O4).
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. 1,2,3-Triazoles are usually prepared following (3+2) cycloaddition protocols. A common technique for unsubstituted triazoles is the Huisgen azide-alkyne 1,3-dipolar cycloaddition: a azide and an alkyne react at high temperature to form a ring. However, the Huisgen strategy produces a mixture of isomers (typically 1,4- and 1,5-disubstituted) when used to produce substituted triazoles.Synthetic Route of C4H3N3O4
Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics