29704-63-0

Basic information

• Product Name: 1,4-Diphenyl-5-amino-1,2,3-triazole
• Synonyms: 1,4-Diphenyl-5-amino-1,2,3-triazole;5-Amino-1,4-diphenyl-1H-1,2,3-triazole;1H-1,2,3-Triazol-5-aMine, 1,4-diphenyl-;3,5-diphenyltriazol-4-amine
• CAS NO: 29704-63-0
• Molecular Formula: C₁₄H₁₂N₄
• Molecular Weight: 236.27188
• Mol File: 29704-63-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 456.9°Cat760mmHg
• Flash Point: 230.1°C
• Appearance: /
• Density: 1.24g/cm³
• Vapor Pressure: 1.56E-08mmHg at 25°C
• Refractive Index: 1.677
• CAS DataBase Reference: 1,4-Diphenyl-5-amino-1,2,3-triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Diphenyl-5-amino-1,2,3-triazole(29704-63-0)
• EPA Substance Registry System: 1,4-Diphenyl-5-amino-1,2,3-triazole(29704-63-0)

Safety Data

• Hazardous Substances Data: 29704-63-0(Hazardous Substances Data)

Usage

General Description

1,4-Diphenyl-5-amino-1,2,3-triazole, also known as diphenylaminotriazole, is a chemical compound with the molecular formula C14H11N5. It is a heterocyclic aromatic compound that contains a triazole ring and two phenyl groups. 1,4-Diphenyl-5-amino-1,2,3-triazole is commonly used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and organic dyes. It is also used as a stabilizer in the plastics industry to improve the resistance of polymers to degradation caused by heat, light, and oxidation. Additionally, 1,4-Diphenyl-5-amino-1,2,3-triazole has potential applications in the development of new materials for electronics and optoelectronics.

InChI:InChI=1/C14H12N4/c15-14-13(11-7-3-1-4-8-11)16-17-18(14)12-9-5-2-6-10-12/h1-10H,15H2

Upstream product

• 53684-55-2 phenyl-(5-phenyl-1H-[1,2,3]triazol-4-yl)-amine 
• 107-21-1 ethylene glycol 
• 140-29-4 phenylacetonitrile 
• 622-37-7 Phenyl azide 

Downstream Products

• 53684-55-2 phenyl-(5-phenyl-1H-[1,2,3]triazol-4-yl)-amine 
• 7664-41-7 ammonia 
• 103-71-9 phenyl isocyanate 
• 62-53-3 aniline 
• 97015-84-4 (5-amino-3,4-diphenyl-pyrrol-2-ylidene)-phenyl-amine 
• 31295-36-0 diphenylmaleimide 
• 29411-28-7 1-Benzoyl-3-phenyltriazene 
• 126159-17-9 1-Phenyl-3-(α-cyanobenzylidene)triazene 
• 126159-12-4 2,N-Diphenyl-2,2-(ethylenedioxy)acetamidine 
• 126159-16-8 1-Phenyl-3-(α-piperidinobenzylidene)triazene 
• 126159-20-4 α-Phenyl-β-cyano-N-phenylcinnamamidine 
• 126159-18-0 2-Imino-2-phenylacetonitrile hydrochloride 
• 126159-13-5 2,N-Diphenyl-2,2-diphenoxyacetamidine 
• 125879-46-1 1-Phenyl-3-(α-aminobenzylidene)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

Azide-acetonitrile "click" reaction triggered by Cs2CO3: The atom-economic, high-yielding synthesis of 5-amino-1,2,3-triazoles

Medicinally important 5-amino-1,2,3-triazoles were synthesized using a novel Cs2CO3-catalyzed azide-acetonitrile[3 + 2]-cycloaddition. Aryl azides and aryl acetonitriles were employed in this transformation resulting in excellent yie