Reaction between 1,2,3-triazole-4,5-dicarboxylic acid and the silver(I) cation was written by Capitan, F.;Salinas, F.;Alonso, E. J.. And the article was included in Boletin de la Sociedad Quimica del Peru in 1973.Category: triazoles This article mentions the following:
1,2,3-Triazole-4,5-dicarboxylic acid reacts with Ag(I) in aqueous HNO3 to give the mono-Ag salt, which has solubility product 1.45 × 10-9. The reaction was useful for determining Ag(I) by potentiometric (σ = ±0.0924) and conductometric (σ = ±0.0332) methods in the absence of Pb(II) and Hg(II), which interfere by forming white precipitates under the reaction conditions. In the experiment, the researchers used many compounds, for example, 1H-1,2,3-Triazole-4,5-dicarboxylic acid (cas: 4546-95-6Category: triazoles).
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.Category: triazoles
Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics