1345842-02-5

Basic information

• Product Name: 4-(4-(tert-butyl)phenyl)-1-(p-tolyl)-1H-1,2,3-triazole
• Synonyms: 4-(4-(tert-butyl)phenyl)-1-(p-tolyl)-1H-1,2,3-triazole
• CAS NO: 1345842-02-5
• Molecular Weight: 291.396
• Mol File: 1345842-02-5.mol

Chemical Properties

• CAS DataBase Reference: 4-(4-(tert-butyl)phenyl)-1-(p-tolyl)-1H-1,2,3-triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-(tert-butyl)phenyl)-1-(p-tolyl)-1H-1,2,3-triazole(1345842-02-5)
• EPA Substance Registry System: 4-(4-(tert-butyl)phenyl)-1-(p-tolyl)-1H-1,2,3-triazole(1345842-02-5)

Safety Data

• Hazardous Substances Data: 1345842-02-5(Hazardous Substances Data)

Upstream product

• 772-38-3 4-tert-Butylphenylacetylene 
• 5720-05-8 4-methylphenylboronic acid 
• 943-27-1 4'-t-butylacetophenone 
• 363588-84-5 N′-(1-(4-(tert-butyl)phenyl)ethylidene)-4-methylbenzenesulfonohydrazide 
• 106-49-0 p-toluidine 

Relevant articles and documents

Copper on chitosan: An efficient and easily recoverable heterogeneous catalyst for one pot synthesis of 1,2,3-triazoles from aryl boronic acids in water at room temperature

Abstract A facile, efficient, and environmentally-friendly one pot protocol has been developed for the synthesis of 1,4-diaryl-1,2,3-triazoles from boronic acids, sodium azide, and acetylenes using copper sulfate immobilized on chitosan as a recyclable he

I2/TBPB mediated oxidative reaction of N-tosylhydrazones with anilines: Practical construction of 1,4-disubstituted 1,2,3-triazoles under metal-free and azide-free conditions

An efficient I2 (20 mol %)/TBPB mediated oxidative formal [4 + 1] cycloaddition of N-tosylhydrazones with anilines via C-N/N-N bond formation and S-N cleavage has been developed. This protocol represents a simple, general, and efficient approac