Alkyl esters of mono- and dicarboxylic acids with 1,2,3-triazole rings was written by Mikhat’ev, B. I.;Shatalov, G. V.;Galkin, V. D.;Kimsanov, B. Kh.;Khuseinov, K.. And the article was included in Doklady Akademii Nauk Tadzhikskoi SSR in 1974.Recommanded Product: 40594-98-7 This article mentions the following:
The triazoledicarboxylates I [R = MeO, EtO, PrO, BuO, Me2CHO, Me2CHCH2O, Me(CH2)4O, Me2CHCH2CH2O, Me(CH2)5O] were prepared by reaction of I (R = Cl) with RH. Esterification of I (R = HO) by refluxing in RH with azeotropic removal of H2O gave II. In the experiment, the researchers used many compounds, for example, Ethyl 1H-1,2,3-triazole-5-carboxylate (cas: 40594-98-7Recommanded Product: 40594-98-7).
Ethyl 1H-1,2,3-triazole-5-carboxylate (cas: 40594-98-7) belongs to triazole derivatives. However, triazoles are also useful in bioorthogonal chemistry, because the large number of nitrogen atoms causes triazoles to react similar to azides. Both the triazoles and their derivatives have significant biological properties including antimicrobial, antiviral, antitubercular, anticancer, anticonvulsant, analgesic, antioxidant, anti-inflammatory, and antidepressant activities.Recommanded Product: 40594-98-7
Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics