In 2020.0 J INORG BIOCHEM published article about HIRSHFELD SURFACE-ANALYSIS; X-RAY; BENZIMIDAZOLE; DERIVATIVES; OXIDATION; ISOMERISM; LIGAND; CO(II); ALPHA; ACID in [Chkirate, Karim; El Hafi, Mohamed; Elotmani, Bouchaib; Essassi, El Mokhtar] Univ Mohammed 5, Fac Sci, Dept Chim, LCOH, BP1014, Rabat 10100, Morocco; [Fettach, Saad; Faouzi, My El Abbes] Univ Mohammed V Rabat, Biopharmaceut & Toxicol Anal Res Team, Lab Pharmacol & Toxicol, Pharmacokinet Res Team,Fac Med & Pharm, Rabat, Morocco; [Karrouchi, Khalid] Mohamed V Univ, Fac Med & Pharm, Lab Analyt Chem & Bromatol, Rabat, Morocco; [Mague, Joel T.] Tulane Univ, Dept Chem, New Orleans, LA 70118 USA; [Radi, Smaail] Univ Mohamed I, Fac Sci, Dept Chim, LCAE, BP 524, Oujda 60000, Morocco; [Adarsh, N. N.; Garcia, Yann] Catholic Univ Louvain, Inst Condensed Matter & Nanosci, Mol Chem Mat & Catalysis IMCN MOST, Pl L Pasteur 1, B-1348 Louvain La Neuve, Belgium in 2020.0, Cited 61.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. Recommanded Product: 61-82-5
Two Cu(II) coordination complexes, C1 and C2 of the formula [Cu(4)2(H2O)(2)], have been prepared by reaction between CuCl2 center dot 2H(2)O and 7-ethoxycarbonylmethyl-5-methyl-1,2,4[1,5-a]pyrimidine (L) in a 1:2 M:L molar ratio. The L molecule decomposes during the reaction process into 7-carboxy-5-methyl-[1,2,4]-triazolo[1,5-a]pyrimidine (4) through an intermediate, ethyl 2,2-dihydroxy-2-(5-methyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-yl) acetate (5), which has been isolated and its crystal structure determined by X-ray diffraction. The X-ray analysis of the single crystals of [Cu(4)(2)(H2O)(2)] obtained from the slow evaporation of EtOH and MeOH, separately, revealed the formation of solvent induced polymorphs C1 and C2, respectively. The primary supramolecular synthon for C1 and C2 are six membered ring, and square shaped hydrogen bonded architecture, respectively. The self-assembly of such synthons resulted in a two dimensional hydrogen bonded sheet supported by O-H center dot center dot center dot O interactions. In addition, the antioxidant properties of the ligands and its complexes were evaluated in vitro using 1,1-diphenyl-2-picrylhydrazyl acid, 2,2′-azino-bis (3-ethylbenzothiazoline-6 sulfonic acid radical scavenging methods and ferric reducing antioxidant power.
Recommanded Product: 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Chkirate, K; Fettach, S; El Hafi, M; Karrouchi, K; Elotmani, B; Mague, JT; Radi, S; Faouzi, ME; Adarsh, NN; Essassi, E; Garcia, Y or concate me.
Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics