1210965-55-1

Basic information

• Product Name: N-benzyl-4-phenylbut-3-yne-1-amine
• Synonyms: N-benzyl-4-phenylbut-3-yne-1-amine
• CAS NO: 1210965-55-1
• Molecular Weight: 235.329
• Mol File: 1210965-55-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-benzyl-4-phenylbut-3-yne-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-4-phenylbut-3-yne-1-amine(1210965-55-1)
• EPA Substance Registry System: N-benzyl-4-phenylbut-3-yne-1-amine(1210965-55-1)

Safety Data

• Hazardous Substances Data: 1210965-55-1(Hazardous Substances Data)

Upstream product

• 27152-63-2 3-(N-Benzylamino)-1-phenylpropan-1-on 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 100-46-9 benzylamine 
• 591-50-4 iodobenzene 
• 85375-43-5 4-methyl-N-(4-phenylbut-3-yn-1-yl)benzenesulfonamide 
• 10229-11-5 4-phenyl-but-3-yn-1-ol 

Downstream Products

• 1258537-92-6 diethyl 2-(benzyl(4-phenylbut-3-yn-1-yl)amino)malonate 
• 854045-93-5 2-(di-tert-butylphosphino)-1,1'-biphenylgold(I) chloride 

Relevant articles and documents

Tert-Butyl Nitrite Promoted Oxidative Intermolecular Sulfonamination of Alkynes to Synthesize Substituted Sulfonyl Pyrroles from the Alkynylamines and Sulfinic Acids

tert-Butyl nitrite promoted oxidative intermolecular sulfonamination of alkynes to synthesize substituted sulfonyl pyrroles from the alkynylamines and sulfinic acids via tandem addition/cyclization was developed. This reaction is performed well by employing tert-butyl nitrite as the oxidant, and various substituted sulfonyl pyrroles are formed in moderate to good yields with no requirement of metal catalysis.

Mechanistic study of gold(I)-catalyzed hydroamination of alkynes: Outer or inner sphere mechanism?

An experimental mechanistic study of the gold(I)-catalyzed hydroamination shows the formation of conformationally flexible auro-iminium salts Au-Im, which originate from the protonation of a vinyl gold species. Rotation around the C-CAu bond is the reason

Synthesis of 3-substituted 3-(trimethylsiloxy)pyrrolidines from β-aminoketones and lithium trimethylsilyldiazomethane

Lithium trimethylsilyldiazomethane reacted with N-benzyl-β-aminoketones at -78 °C in THF to give 3-substituted 1-benzyl-3-(trimethylsiloxy)pyrrolidines in moderate to good yields.