14331-64-7

Basic information

• Product Name: 4H-1,2,4-Triazole, 3,4-diphenyl-
• CAS NO: 14331-64-7
• Molecular Formula: C14H11N3
• Molecular Weight: 221.261
• Mol File: 14331-64-7.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 4H-1,2,4-Triazole, 3,4-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 4H-1,2,4-Triazole, 3,4-diphenyl-(14331-64-7)
• EPA Substance Registry System: 4H-1,2,4-Triazole, 3,4-diphenyl-(14331-64-7)

Safety Data

• Hazardous Substances Data: 14331-64-7(Hazardous Substances Data)

Upstream product

• 6596-82-3 4,5-diphenyl-4H-1,2,4-triazole-3-thiol 
• 5351-69-9 4-Phenyl-3-thiosemicarbazide 
• 81816-99-1 N-phenylsulfonyl-N''-phenylbenzamidrazone 
• 62-53-3 aniline 
• 825-56-9 2-phenyl-1,3,4-oxadiazole 
• 142-04-1 aniline hydrochloride 
• 90959-31-2 C₂₀H₁₉N₃O₂S 
• 19958-26-0 benzoic acid-(anilinomethylene-hydrazide) 
• 6596-82-3 4,5-diphenyl-2,4-dihydro-[1,2,4]triazole-3-thione 
• 913329-62-1 (E)-2-benzylidene-N-phenylhydrazinecarbothioamide 
• 100-52-7 benzaldehyde 
• 20033-56-1 [(ethylsulfanyl)phenylmethylidene]aniline 
• 624-84-0 formic acid hydrazide 
• 636-04-4 N-Phenylbenzothioamide 

Downstream Products

• 1262790-97-5 3-bromo-4,5-diphenyl-4H-1,2,4-triazole 
• 57575-71-0 3,4-diphenyl-5-p-tolyl-4H-1,2,4-triazole 
• 1187772-50-4 3,4-diphenyl-5-(phenylethynyl)-4H-1,2,4-triazole 
• 1173178-67-0 3-(4-butylphenyl)-4,5-diphenyl-4H-1,2,4-triazole 
• 57575-77-6 4-(4,5-diphenyl-4H-1,2,4-triazol-3-yl)benzonitrile 
• 102469-83-0 3-(4-methoxyphenyl)-4,5-diphenyl-4H-1,2,4-triazole 
• 4073-72-7 3,4,5-triphenyl-1,2,4-triazole 
• 56999-71-4 4,5-diphenyl-4H-1,2,4-triazol-3-ylmethanol 

Relevant articles and documents

Recyclization of 1,3,4-oxadiazoles and bis-1,3,4-oxadiazoles into 1,2,4-triazole derivatives. Synthesis of 5-unsubstituted 1,2,4-triazoles

Efficient methods have been developed for obtaining precursors of stable carbenes, viz. 5-unsubstituted 3,4-diaryl-1,2,4-triazoles and 3,3′- or 4,4′-bridge linked bis-1,2,4-triazoles, by the recyclization of 5-unsubstituted 1,3,4-oxadiazoles or p-phenylen

Two green iridium(iii) complexes containing the electron-transporting group of 4-phenyl-4H-1,2,4-triazole for highly efficient OLEDs

Two new iridium(iii) cyclometalated complexes (Ir-TN3T and Ir-TN4T) with 2′,6′-bis(trifluoromethyl)-2,3′-bipyridine (TN3T) and 2′,6′-bis(trifluoromethyl)-2,4′-bipyridine (TN4T) as the cyclometalated ligands and

Tunable protic ionic liquids as solvent-catalysts for improved synthesis of multiply substituted 1,2,4-triazoles from oxadiazoles and organoamines

More than green alternatives to traditional volatile molecular organic solvents, protic ionic liquids as dual solvent-catalysts have been successfully used to promote reactions of organoamines with oxadiazoles to afford sterically hindered 1,2,4-triazoles. Among the tested protic ionic liquids, pyridinium trifluoroacetate and acetate showed the highest efficiency for the reactions of arylamines and alkylamines, respectively, indicating that tunable catalysis could be readily effected with protic ionic liquid solvent-catalysts by simply tuning their cation and anion counterparts. A general and efficient approach has been developed for synthesis of multiply substituted 1,2,4-triazoles based on the tunable protic ionic liquid solvent-catalyst systems.