68809-41-6

Basic information

• Product Name: 4-(4-methoxyphenyl)-1-phenyl-1H-[1,2,3]triazole
• Synonyms: 4-(4-methoxyphenyl)-1-phenyl-1H-[1,2,3]triazole
• CAS NO: 68809-41-6
• Molecular Weight: 251.288
• Mol File: 68809-41-6.mol
• Article Data: 28

Chemical Properties

• CAS DataBase Reference: 4-(4-methoxyphenyl)-1-phenyl-1H-[1,2,3]triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-methoxyphenyl)-1-phenyl-1H-[1,2,3]triazole(68809-41-6)
• EPA Substance Registry System: 4-(4-methoxyphenyl)-1-phenyl-1H-[1,2,3]triazole(68809-41-6)

Safety Data

• Hazardous Substances Data: 68809-41-6(Hazardous Substances Data)

Upstream product

• 5703-26-4 4-Methoxyphenylacetaldehyde 
• 622-37-7 Phenyl azide 
• 3989-14-8 (4-methoxyphenylethynyl)trimethylsilane 
• 108-86-1 bromobenzene 
• 768-60-5 4-methoxyphenylacetylen 
• 62-53-3 aniline 
• 591-50-4 iodobenzene 
• 2196-99-8 2-chloro-1-(4-methoxyphenyl)ethanone 
• 98-80-6 phenylboronic acid 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 32117-52-5 1-(1-(4-methoxyphenyl)ethylidene)-2-tosylhydrazine 
• 696-62-8 para-iodoanisole 
• 369-57-3 benzenediazonium tetrafluoroborate 

Relevant articles and documents

CuO–NiO bimetallic nanoparticles supported on graphitic carbon nitride with enhanced catalytic performance for the synthesis of 1,2,3-triazoles, bis-1,2,3-triazoles, and tetrazoles in parts per million level

The unification of CuCl2·2H2O and NiCl2·6H2O with the support of graphitic carbon nitride yielded to form an efficient, synergistic, bimetallic nano-catalyst CuO–NiO@g-C3N4. FT-IR, SEM, TEM

Iodine-mediated C-N and N-N bond formation: A facile one-pot synthetic approach to 1,2,3-triazoles under metal-free and azide-free conditions

A novel strategy towards the synthesis of 1,4-disubstituted 1,2,3-triazoles via C-N and N-N bond formation has been demonstrated under transition metal-free and azide-free conditions. These 1,2,3-triazoles were obtained in a regioselective manner from commercially available anilines, aryl alkenes/aryl alkynes and N-tosylhydrazines using I2 under O2 atmosphere. Broad substrate scope, milder reaction conditions, good to moderate yields and clean protocol are the notable features of the method. Moreover, this protocol is amenable for the generation of a library of medicinally important key building blocks.

Application of two magnetic nanoparticle-supported copper(I) catalysts for the synthesis of triazole derivatives

Catalytic performance of two magnetically recoverable copper(I) complexes is reported for the synthesis of 1,2,3-triazole derivatives. Boronic acids and alkyl halides, in the presence of either catalyst, react with terminal alkynes and NaN3, fo