51335-60-5

Basic information

• Product Name: 1,3-diphenyl-5-propyl-1H-1,2,4-triazole
• Synonyms: 1,3-diphenyl-5-propyl-1H-1,2,4-triazole
• CAS NO: 51335-60-5
• Molecular Weight: 263.342
• Mol File: 51335-60-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,3-diphenyl-5-propyl-1H-1,2,4-triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-diphenyl-5-propyl-1H-1,2,4-triazole(51335-60-5)
• EPA Substance Registry System: 1,3-diphenyl-5-propyl-1H-1,2,4-triazole(51335-60-5)

Safety Data

• Hazardous Substances Data: 51335-60-5(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 109-73-9 N-butylamine 
• 100-63-0 phenylhydrazine 
• 123-72-8 butyraldehyde 
• 588-64-7 benzaldehyde phenylhydrazone 
• 586-96-9 Nitrosobenzene 
• 100-46-9 benzylamine 
• 33243-87-7 N-butyryl-benzimidic acid ethyl ester 
• 5333-86-8 ethyl benzimidate hydrochloride 

Relevant articles and documents

Electrosynthesis of 1,3,5-trisubstituted 1,2,4-triazoles from phenylhydrazine, aldehydes and amines under mild conditions

A simple and convenient method for the electrosynthesis of 1,3,5-trisubstituted 1,2,4-triazoles with three components of phenylhydrazine, aldehydes and amines has been established. The electrolysis could be smoothly carried out at room temperature without additional strong oxidants and catalysts to afford the target product in good yields. This electrochemical route effectively extends synthetic field of 1,2,4-triazole derivatives.

N-Aminations of Benzylamines and Alicyclic Amines with Nitrosoarenes to Hydrazones and Hydrazides

Unlike other alkylamines, benzylamines upon reaction with a nitrosoarene undergo oxidation to the corresponding imines. A direct amination of benzylamines, which was difficult to achieve due to its facile oxidation, to the corresponding hydrazones is reported. A wide variety of benzylamines and N-heterocycles were reacted with nitrosoarenes to provide structurally diverse hydrazones and hydrazides, respectively. Moreover, the direct N-amination reaction was applied to the one-pot synthesis of triazoles.