72680-08-1

Basic information

• Product Name: ethyl 5-amino-1-p-tolyl-1H-1,2,3-triazole-4-carboxylate
• Synonyms: ethyl 5-amino-1-p-tolyl-1H-1,2,3-triazole-4-carboxylate
• CAS NO: 72680-08-1
• Molecular Weight: 246.269
• Mol File: 72680-08-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: ethyl 5-amino-1-p-tolyl-1H-1,2,3-triazole-4-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 5-amino-1-p-tolyl-1H-1,2,3-triazole-4-carboxylate(72680-08-1)
• EPA Substance Registry System: ethyl 5-amino-1-p-tolyl-1H-1,2,3-triazole-4-carboxylate(72680-08-1)

Safety Data

• Hazardous Substances Data: 72680-08-1(Hazardous Substances Data)

Upstream product

• 2028-84-4 p-methylbenzenediazonium chloride 
• 106-49-0 p-toluidine 
• 2101-86-2 p-methylazidobenzene 
• 105-56-6 ethyl 2-cyanoacetate 
• 5873-88-1 2-Ethoxycarbonyl-S-methylthioacetamidate hydrochloride 
• 13621-50-6 ethoxycarbonylthioacetamide 
• 122380-11-4 2-Ethoxycarbonyl-N-(4-tolyl)acetamidine hydrochloride 

Downstream Products

• 1160050-83-8 5-(p-tolylamino)-2H-1,2,3-triazol-4-carbohydrazide 
• 1026253-69-9 5-amino-1-p-tolyl-1H-[1,2,3]triazole-4-carboxylic acid 
• 272123-49-6 1-(p-methylphenyl)-4-ethoxycarbonyl-5-[(triphenylphosphoranylidene)amino]-1,2,3-triazole 
• 62469-98-1 ethyl 5-anilino-1H-v-triazole-4-carboxylate 

Relevant articles and documents

Synthesis and in vitro and in silico studies of 1H- and 2H-1,2,3-triazoles as antichagasic agents

1,2,3-triazole heterocycles stand out in medicinal chemistry for having great structural diversity and bioactivities. In this study, two series of triazoles were synthesized. One was obtained by the 1,3-dipolar cycloaddition reaction between ethyl cyanoac

Synthesis and crystal structure of (5-methyl-3-phenyl-1h-pyrazol-1-yl)-[5- (p-tolylamino)-2h-1,2,3-triazol-4-yl]methanone

(5-Methyl-3-phenyl-1H-pyrazol-1-yl)-[5-(p-tolylamino)-2H-1,2, 3-triazol-4-yl]methanone was synthesized and characterized by 1H NMR, MS and IR spectra data. The structure of title compound was identified by X-ray diffraction. Compound, C20

Studies on v-Triazoles. Part I: Synthesis of 4,9-Dihydro-9-oxo-1H-v-triazolo quinolines by cyclization of 5-arylamino-v-triazole-4-carboxylic acids with polyphosphoric acid.

The cyclization of 5-arylamino-v-triazole-4-carboxylic acids with polyphosphoric acid leads to high yields of the corresponding 4,9-dihydro-9-oxo-v-triazolo quinolines which are potent antiallergic agents.