1328889-67-3

Basic information

• Product Name: N-(1,2-diphenylbuta-2,3-dien-1-yl)aniline
• Synonyms: N-(1,2-diphenylbuta-2,3-dien-1-yl)aniline
• CAS NO: 1328889-67-3
• Molecular Weight: 297.4
• Mol File: 1328889-67-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(1,2-diphenylbuta-2,3-dien-1-yl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-(1,2-diphenylbuta-2,3-dien-1-yl)aniline(1328889-67-3)
• EPA Substance Registry System: N-(1,2-diphenylbuta-2,3-dien-1-yl)aniline(1328889-67-3)

Safety Data

• Hazardous Substances Data: 1328889-67-3(Hazardous Substances Data)

Upstream product

• 538-51-2 benzylidene phenylamine 
• 1794-48-5 1-bromo-3-phenylprop-2-yne 
• 98-86-2 acetophenone 

Downstream Products

• 1294009-49-6 1,2,3-triphenyl-3-pyrroline 
• 1328889-81-1 4-chloro-1,2,3-triphenyl-3-pyrroline 
• 1328889-69-5 C₂₂H₁₈BrN 
• 1328889-74-2 1,2,3,4-tetraphenyl-3-pyrroline 
• 1328889-76-4 4-tert-butyldimethylsilylethynyl-1,2,3-triphenyl-3-pyrroline 
• 1328889-78-6 4-chloro-1,2,3-triphenylpyrrole 
• 6932-23-6 1,2,3,4-tetraphenyl-1H-pyrrole 

Relevant articles and documents

A Tetraarylpyrrole-Based Phosphine Ligand for the Palladium-Catalyzed Amination of Aryl Chlorides

A tetraarylpyrrole-based phosphine ligand L1 in combination with Pd(dba)2 provided a catalyst for the Buchwald-Hartwig amination reaction. A variety of amines were rapidly coupled with aryl chlorides at a Pd loading of 0.5 mol%. The selective monoarylation of aliphatic primary amines was achieved in the presence of 0.8 equiv. water. Comparison experiments were also conducted, which revealed that the catalytic activity of L1 is superior to representative phosphine ligands in the Pd-catalyzed C?N coupling of various amines. (Figure presented.).

Silver-catalyzed intramolecular chloroamination of allenes: Easy access to functionalized 3-pyrroline and pyrrole derivatives

A 1,10-phenanthroline-ligated cationic silver complex allows the intramolecular chloroamination of allenes with N-chlorosuccinimide using 2,6-lutidine as a base. This process proceeds under mild conditions and can tolerate a variety of functional groups.