106736-30-5

Basic information

• Product Name: 1-(4-nitrophenyl)-4-phenyl-1H-1,2,3-triazol-5-amine
• Synonyms: 1-(4-nitrophenyl)-4-phenyl-1H-1,2,3-triazol-5-amine
• CAS NO: 106736-30-5
• Molecular Weight: 281.274
• Mol File: 106736-30-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(4-nitrophenyl)-4-phenyl-1H-1,2,3-triazol-5-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-nitrophenyl)-4-phenyl-1H-1,2,3-triazol-5-amine(106736-30-5)
• EPA Substance Registry System: 1-(4-nitrophenyl)-4-phenyl-1H-1,2,3-triazol-5-amine(106736-30-5)

Safety Data

• Hazardous Substances Data: 106736-30-5(Hazardous Substances Data)

Upstream product

• 1516-60-5 4-nitrophenyl azide 
• 140-29-4 phenylacetonitrile 
• 106736-31-6 (4-nitro-phenyl)-(5-phenyl-1H-[1,2,3]triazol-4-yl)-amine 
• 71-43-2 benzene 
• 67-64-1 acetone 
• 141-78-6 ethyl acetate 
• 107-21-1 ethylene glycol 
• 64-17-5 ethanol 

Downstream Products

• 106736-31-6 (4-nitro-phenyl)-(5-phenyl-1H-[1,2,3]triazol-4-yl)-amine 
• 123035-36-9 3-(α-cyano)benzylidene-1-(4-nitrophenyl)triazene 

Relevant articles and documents

Designing a new basic ionic liquid [DHIM][OH] as a task specific bifunctional catalyst for facile microwave assisted metal free synthesis of 5-amino-1,2,3-triazoles

A green protocol for the synthesis of a series of 5-amino-1,2,3-triazoles from benzyl cyanide and phenyl azide derivatives catalyzed by the novel bifunctional ionic liquid [DHIM][OH] under microwave irradiation has been developed. The bifunctional ionic l

INFLUENCE OF ELECTRON-WITHDRAWING N-1 SUBSTITUENTS ON THE THERMAL BEHAVIOUR OF S-AZIDO-1,2,3-TRIAZOLES

5-Amino-1,2,3-triazoles (7), possessing a strong electron-withdrawing N-1 substituent, cannot be converted into the corresponding azides by the diazotization method, but the diazo transfer on the conjugate bases with tosyl azide proceeds smoothly and was