1250525-60-0

Basic information

• Product Name: 1-benzyl-4-(2-bromoethyl)-1H-1,2,3-triazole
• Synonyms: 1-benzyl-4-(2-bromoethyl)-1H-1,2,3-triazole
• CAS NO: 1250525-60-0
• Molecular Weight: 266.14
• Mol File: 1250525-60-0.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1-benzyl-4-(2-bromoethyl)-1H-1,2,3-triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzyl-4-(2-bromoethyl)-1H-1,2,3-triazole(1250525-60-0)
• EPA Substance Registry System: 1-benzyl-4-(2-bromoethyl)-1H-1,2,3-triazole(1250525-60-0)

Safety Data

• Hazardous Substances Data: 1250525-60-0(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 38771-21-0 4-bromobut-1-yne 
• 622-79-7 benzyl azide 

Downstream Products

• 1314581-69-5 4-{2-[4-(2-azidoethyl)-1H-1,2,3-triazol-1-yl]ethyl}-1-[2-(1-benzyl-1H-1,2,3-triazol-4-yl)ethyl]-1H-1,2,3-triazole 
• 1314581-71-9 1-[2-(1-benzyl-1H-1,2,3-triazol-4-yl)ethyl]-4-octyl-1H-1,2,3-triazole 
• 1314581-72-0 1-[2-(1-benzyl-1H-1,2,3-triazol-4-yl)ethyl]-4-phenyl-1H-1,2,3-triazole 
• 1314581-73-1 1-[2-(1-benzyl-1H-1,2,3-triazol-4-yl)ethyl]-4-(p-tolyl)-1H-1,2,3-triazole 
• 1314581-78-6 1-[2-(1-benzyl-1H-1,2,3-triazol-4-yl)ethyl]-4-[2-(4-phenyl-1H-1,2,3-triazol-1-yl)ethyl]-1H-1,2,3-triazole 
• 1314581-79-7 1-[2-(1-benzyl-1H-1,2,3-triazol-4-yl)ethyl]-4-{2-[4-(thiophen-3-yl)-1H-1,2,3-triazol-1-yl]ethyl}-1H-1,2,3-triazole 
• 1314581-82-2 1-(2-(1-benzyl-1H-1,2,3-triazol-4-yl)ethyl)-4-(2-(4-(2-(4-phenyl-1H-1,2,3-triazol-1-yl)ethyl)-1H-1,2,3-triazol-1-yl)ethyl)-1H-1,2,3-triazole 
• 1314581-61-7 4-(2-azidoethyl)-1-benzyl-1H-1,2,3-triazole 
• 1314581-63-9 1-[2-(1-benzyl-1H-1,2,3-triazol-4-yl)ethyl]-4-(2-bromoethyl)-1H-1,2,3-triazole 
• 1314581-65-1 4-(2-azidoethyl)-1-[2-(1-benzyl-1H-1,2,3-triazol-4-yl)ethyl]-1H-1,2,3-triazole 
• 1314581-67-3 1-[2-(1-benzyl-1H-1,2,3-triazol-4-yl)ethyl]-4-{2-[4-(2-bromoethyl)-1H-1,2,3-triazol-1-yl]ethyl}-1H-1,2,3-triazole 

Relevant articles and documents

A facile synthesis of N-C linked 1,2,3-triazole-oligomers

The synthesis of the title oligomers was performed by means of an iterative sequence of 1,3-dipolar cycloaddition reactions of appropriate azides, starting from commercial 4-bromo-1-butyne as a key intermediate.

Copper complexes bearing an NHC-calixarene unit: Synthesis and application in click chemistry

The synthesis of N-heterocyclic carbene (NHC) copper complexes supported by calix[4]arene is reported. Mono-substituted calix[4]arene was prepared through conventional procedures, followed by the attachment of an imidazolyl group to create the precursor o

Glycerol: A biorenewable solvent for base-free Cu(i)-catalyzed 1,3-dipolar cycloaddition of azides with terminal and 1-iodoalkynes. Highly efficient transformations and catalyst recycling

The combination of CuI and glycerol exhibits a versatile and high catalytic activity in the Huisgen cycloaddition of azides and terminal or 1-iodoalkynes under standard bench experimental conditions (room temperature, under air and in the absence of a bas