1294505-32-0

Basic information

• Product Name: N-benzyl-N-(2-bromobenzyl)-1,3-diphenylprop-2-yn-1-amine
• Synonyms: N-benzyl-N-(2-bromobenzyl)-1,3-diphenylprop-2-yn-1-amine
• CAS NO: 1294505-32-0
• Molecular Weight: 466.42
• Mol File: 1294505-32-0.mol

Chemical Properties

• CAS DataBase Reference: N-benzyl-N-(2-bromobenzyl)-1,3-diphenylprop-2-yn-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-N-(2-bromobenzyl)-1,3-diphenylprop-2-yn-1-amine(1294505-32-0)
• EPA Substance Registry System: N-benzyl-N-(2-bromobenzyl)-1,3-diphenylprop-2-yn-1-amine(1294505-32-0)

Safety Data

• Hazardous Substances Data: 1294505-32-0(Hazardous Substances Data)

Upstream product

• 65185-56-0 N-benzyl-1-(2-bromophenyl)methanamine 
• 100-52-7 benzaldehyde 
• 536-74-3 phenylacetylene 

Downstream Products

• 1294505-49-9 (Z)-2-benzyl-4-benzylidene-3-phenyl-1,2,3,4-tetrahydroisoquinoline 

Relevant articles and documents

Synthesis of [1,2,3]-triazolo[1,5-a][1,4]benzodiazepines via an unprecedented one-pot Cu-catalyzed azidation-cyclization reaction

A novel three-step approach leading to [1,2,3]-triazolo[1,5-a][1,4] benzodiazepines in moderate to good yields has been developed. The key step is an unprecedented one-pot Cu-catalyzed azidation-cyclization reaction of ortho-bromobenzylpropargylamines.

Synthesis of functionalized tetrahydroisoquinolines via palladium-catalyzed 6-exo-dig carbocyclization of 2-bromo-N-propargylbenzylamines

An efficient twostep synthetic strategy for tetrahydroisoquinolines has been described. The first step involves CuI catalyzed three-component coupling reaction of terminal alkyne, aldehyde and amine that provides the requisite propargyl amine. Regio- and