223645-69-0Relevant academic research and scientific papers
A facile and solvent-free synthesis of 3,5 -disubstituted-4-amino-1,2,4-triazoles by reactions of aromatic nitriles with hydrazine
Ikemi, Yukio,Hayashi, Naoto,Kakehi, Akikazu,Matsumoto, Kiyoshi
, p. 439 - 442 (2002)
A variety of 3, 5-disubstituted-4-amino-1,2,4-triazoles were prepared by reactions of aromatic nitriles with hydrazine monohydrate. The structure of 3,5-diphenyl-4-amino-1,2,4-triazole was established by an X-ray analysis.
Novel bent-core mesogenic of 4-amino-triazole derivatives: synthesis, characterization and liquid crystalline study
Tomi, Ivan Hameed R.,Al-Daraji, Ali Hussein R.,Al-Qaisi, Ziad Hussein J.,Al-Heetimi, Dhafir T.A.,Al-Qaisi, Alaa Hussein J.
, p. 4390 - 4399 (2016)
The synthesis, characterization and mesomorphism of twelve new bent-shaped mesogens containing 4-amino-1,2,4-triazole as a central rigid core (II)nare reported. The amino triazole derivatives were characterized by1H,13C NM
The hydroxylic position mediated the luminescent properties based on 4-amino-4H-1,2,4-triazole: Syntheses, crystal structures and Hirshfeld analyses
Chen, Xiao-Min,Chen, Xu-Kai,Liu, Xing-Rui,Sun, Wen-Chao,Tang, Gui-Mei,Wang, Yong-Tao,Wu, Yu-Song,Xi, Yu-Rong,Xue, Yun-Kai
, (2021/06/21)
A set of compounds based on 4-amino-4H-1,2,4-triazole group, namely, x,x'-(4-amino-4H-1,2,4-triazole-3,5-diyl) diphenol [x ?= ?2 (1), x ?= ?3 (2), x ?= ?4 (3)], were obtained through reacting a set of cyano-phenol and hydrazine under the solvothermal cond
The substituent effect on the luminescent properties of a set of 4-amino-4H-1,2,4-triazole: Syntheses, crystal structures and Hirshfeld analyses
Chen, Xiao-Min,Chen, Xu-Kai,Tang, Gui-Mei,Wang, Shi-Ning,Wang, Yong-Tao,Wu, Yu-Song,Xi, Yu-Rong
, (2021/06/26)
A set of compounds based on 4-amino-4H-1,2,4-triazole group, namely, 4,4′-(4-amino-4H-1,2,4-triazole-3,5-diyl)dibenzoic acid (1), 4,4′-(4-amino-4H-1,2,4-triazole-3,5-diyl)dianiline (2), 4,4′-(4-amino-4H-1,2,4-triazole-3,5-diyl)diphenol (3), were obtained
Accelerated synthesis of 3,5-disubstituted 4-amino-1,2,4-triazoles under microwave irradiation
Bentiss, Fouad,Lagrenée, Michel,Barbry, Didier
, p. 1539 - 1541 (2007/10/03)
A number of symmetrically 3,5-disubstituted 4-amino-1,2,4-triazoles are quickly prepared by the reaction of aromatic nitriles on hydrazine dihydrochloride in the presence of an excess of hydrazine hydrate in ethylene glycol under microwave irradiation. (C
A simple one step synthesis of new 3,5-disubstituted-4-amino-1,2,4- triazoles
Bentiss,Lagrenee,Traisnel,Mernari,Elattari
, p. 149 - 152 (2007/10/03)
A number of symmetrically 3,5-disubstituted 4-amino-1,2,4-triazoles have been prepared by the reaction of aromatic nitriles with hydrazine dihydrochloride or sulfate with an excess of hydrazine hydrate in ethylene or diethylene glycol under a nitrogen atm
