5533-73-3

Basic information

• Product Name: 4,5-Diphenyl-1H-1,2,3-triazole
• Synonyms: 4,5-Diphenyl-1H-1,2,3-triazole
• CAS NO: 5533-73-3
• Molecular Formula: C₁₄H₁₁N₃
• Molecular Weight: 249.3056
• Mol File: 5533-73-3.mol
• Article Data: 15

Chemical Properties

• Melting Point: 133-135 °C
• Boiling Point: 448.4°Cat760mmHg
• Flash Point: 225°C
• Appearance: /
• Density: 1.14g/cm³
• Vapor Pressure: 3.1E-08mmHg at 25°C
• Refractive Index: 1.545
• PKA: 8.07±0.70(Predicted)
• CAS DataBase Reference: 4,5-Diphenyl-1H-1,2,3-triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 4,5-Diphenyl-1H-1,2,3-triazole(5533-73-3)
• EPA Substance Registry System: 4,5-Diphenyl-1H-1,2,3-triazole(5533-73-3)

Safety Data

• Hazardous Substances Data: 5533-73-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H19NO3/c1-17-12-6-3-10(9-13(12)18-2)7-8-15-14(16)11-4-5-11/h3,6,9,11H,4-5,7-8H2,1-2H3,(H,15,16)

Upstream product

• 40788-61-2 1-amino-4,5-diphenyl-1,2,3-triazole 
• 5162-99-2 2,3-Diphenylthiirene 1,1-dioxide 
• 42353-58-2 1-(1,2-diphenyl-vinyl)-pyrrolidine 
• 26386-88-9 diphenyl phosphoryl azide 
• 73558-58-4 4H-2,6-Diphenyl-1,3,4,5-thiatriazine 1,1-dioxide 
• 501-65-5 diphenyl acetylene 
• 64781-77-7 4-diazo-5-phenyl-4H-1,2,3-triazole 
• 71-43-2 benzene 
• 61588-68-9 N-(4,5-diphenyl-[1,2,3]triazol-1-yl)-benzamide 
• 67-63-0 isopropyl alcohol 
• 908094-04-2 phenyldiazomethane 
• 889095-93-6 4,5-diphenyl-1-[2-(toluene-4-sulfonyl)-ethyl]-1H-[1,2,3]triazole 
• 73558-57-3 2,6-Diphenyl-4-benzoyl-1,3,4,5-thiatriazine 1,1-dioxide 
• 69754-64-9 4-<(E)-1,2-diphenylvinyl>-2,6-diphenyl-1,3,4,5-thiatriazine 1,1-dioxide 

Downstream Products

• 193742-76-6 2-(9-Hydroxynonyl)-4,5-diphenyl-1,2,3-triazole 
• 142498-35-9 2-(6-Ethoxycarbonylhexyl)-4,5-diphenyl-1,2,3-triazole 
• 142498-38-2 1-(8-Bromooctyl)-4,5-diphenyl-1,2,3-triazole 
• 142498-37-1 2-(8-Bromooctyl)-4,5-diphenyl-1,2,3-triazole 
• 1392498-77-9 4,5-diphenyl-2-(trifluoromethyl)-2H-1,2,3-triazole 
• 1392498-76-8 4,5-diphenyl-1-(trifluoromethyl)-1H-1,2,3-triazole 

Relevant articles and documents

Iodine-Mediated Condensation–Cyclization of α-Azido Ketones with p-Toluenesulfonyl Hydrazide for Synthesis of 4-Aryl-NH-1,2,3-Triazoles

A molecular iodine mediated condensation–cyclization reaction for the synthesis of 4-aryl-NH-1,2,3-triazoles has been developed from readily available α-azido acetophenones and p-toluenesulfonyl hydrazide. This reaction provides a metal-free strategy for the sequential formation of C–N and N–N bonds in mild condition.

CONDENSED CYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

A condensed cyclic compound represented by Formula 1: [in-line-formulae]Ar1-(L1)m1-Ar2??Formula 1[/in-line-formulae]wherein, in Formula 1, Ar1, Ar2, L1, and ml are the same as described in the specification.

Condensed cyclic compound and organic light-emitting device including the same

Disclosed are a condensed-cyclic compound and an organic light-emitting device comprising the same. The condensed-cyclic compound is represented by chemical formula 1. The condensed-cyclic compound has excellent electrical properties and thermal stability. The organic light-emitting device comprising the condensed-cyclic compound can have a low driving voltage, high efficiency, high luminance, long lifespan, and properties of high color purity.COPYRIGHT KIPO 2016