126800-09-7

Basic information

• Product Name: 1-(4-bromobenzyl)-4-phenyl-1H-1,2,3-triazole
• Synonyms: 1-(4-bromobenzyl)-4-phenyl-1H-1,2,3-triazole
• CAS NO: 126800-09-7
• Molecular Weight: 314.184
• Mol File: 126800-09-7.mol
• Article Data: 110

Chemical Properties

• CAS DataBase Reference: 1-(4-bromobenzyl)-4-phenyl-1H-1,2,3-triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-bromobenzyl)-4-phenyl-1H-1,2,3-triazole(126800-09-7)
• EPA Substance Registry System: 1-(4-bromobenzyl)-4-phenyl-1H-1,2,3-triazole(126800-09-7)

Safety Data

• Hazardous Substances Data: 126800-09-7(Hazardous Substances Data)

Upstream product

• 536-74-3 phenylacetylene 
• 932-88-7 1-iodo-2-phenylethyne 
• 589-15-1 1-bromomethyl-4-bromobenzene 
• 75-52-5 nitromethane 
• 100-52-7 benzaldehyde 
• 107047-10-9 p-bromobenzylazide 
• 74489-49-9 4-azidobenzyl bromide 
• 5651-88-7 phenyl propargyl sulfide 
• 70978-37-9 1-(azidomethyl)-4-methoxybenzene 
• 589-17-3 p-bromobenzyl chloride 

Downstream Products

• 1239481-15-2 3-(4-((4-phenyl-1H-1,2,3-triazol-1-yl)methyl)phenyl)pyridine 

Relevant articles and documents

Copper immobilized onto polymer-coated magnetic nanoparticles as recoverable catalyst for ‘click’ reaction

Copper supported on polymer-coated magnetic nanoparticles was designed and synthesized as a separable heterogeneous catalyst. The catalyst was fully characterized using several techniques such as Fourier transform infrared and energy-dispersive X-ray spec

Multi-component reaction for the preparation of 1,5-disubstituted 1,2,3-triazoles by in-situ generation of azides and nickel-catalyzed azide-alkyne cycloaddition

An efficient one-pot procedure combining bromide conversion into azide followed by NiAAC for the preparation of 1,5-disubstituted 1,2,3-triazoles has been developed. This procedure prevents the use of isolated azides, which are insufficiently commercially

Synthesis of copper containing polyaniline composites through interfacial polymerisation: An effective catalyst for Click reaction at room temperature

Polyaniline (PANI) supported Cu (Cu/PANI) catalyst served as an efficient heterogeneous catalyst for the regioselective synthesis of 1,4-disubstituted-1H-1,2,3-triazoles via click chemistry approach. Herein, we have illustrated the development of two copp