1562381-71-8

Basic information

• Product Name: N,4-dimethyl-N-(4-(2-methyl-1H-indol-3-yl)-5-phenylfuran-2-yl)benzenesulfonamide
• Synonyms: N,4-dimethyl-N-(4-(2-methyl-1H-indol-3-yl)-5-phenylfuran-2-yl)benzenesulfonamide
• CAS NO: 1562381-71-8
• Molecular Weight: 456.565
• Mol File: 1562381-71-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N,4-dimethyl-N-(4-(2-methyl-1H-indol-3-yl)-5-phenylfuran-2-yl)benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,4-dimethyl-N-(4-(2-methyl-1H-indol-3-yl)-5-phenylfuran-2-yl)benzenesulfonamide(1562381-71-8)
• EPA Substance Registry System: N,4-dimethyl-N-(4-(2-methyl-1H-indol-3-yl)-5-phenylfuran-2-yl)benzenesulfonamide(1562381-71-8)

Safety Data

• Hazardous Substances Data: 1562381-71-8(Hazardous Substances Data)

Upstream product

• 586-96-9 Nitrosobenzene 
• 1562381-51-4 (E)-N-(4-(4-methoxyphenyl)but-3-en-1-yn-1-yl)-N,4-dimethylbenzenesulfonamide 
• 100-52-7 benzaldehyde 
• 1608-03-3 (E)-but-1-en-3-yn-1-ylbenzene 
• 95-20-5 2-methyl-1H-indole 
• 1562381-58-1 4-hydroxy-N-methyl-N',4-diphenyl-N-tosylbut-2-ynimidamide 
• 1562381-49-0 (E)-N-(4-(4-chlorophenyl)but-3-en-1-yn-1-yl)-N,4-dimethylbenzenesulfonamide 
• 1562381-11-6 (E)-N-methyl-N-(4-phenylbut-3-en-1-yn-1-yl)methanesulfonamide 
• 1562381-56-9 (E)-N-(4-cyclohexenylbut-3-en-1-ynyl)-N,4-dimethylbenzenesulfonamide 
• 1562381-55-8 N,4-dimethyl-N-((3E,5E)-6-phenylhexa-3,5-dien-1-yn-1-yl)benzenesulfonamide 
• 1384432-41-0 (E)-N-methyl-N-(3-methyl-4-phenylbut-3-en-1-yn-1-yl)methanesulfonamide 
• 1562381-54-7 N-((3E,5E)-6-(furan-2-yl)hexa-3,5-dien-1-ynyl)-N,4-dimethylbenzenesulfonamide 
• 640-61-9 N-methyl-p-toluenesulfonylamide 

Relevant articles and documents

Zn(II)- or Ag(I)-catalyzed 1,4-metathesis reactions between 3-en-1-ynamides and nitrosoarenes

Catalyst-dependent metathesis reactions between 3-en-1-ynamides and nitrosoarenes are described. Particularly notable are the unprecedented 1,4-metathesis reactions catalyzed by Ag(I) or Zn(II) to give 2-propynimidamides and benzaldehyde derivatives. With 3-en-1-ynamides bearing a cycloalkenyl group, 1,4-oxoimination products were produced efficiently. We have developed metathesis/alkynation cascades for unsubstituted 2-propynimidamides and benzaldehyde species generated in situ, to manifest 1,4-hydroxyimination reactions of 3-en-1-ynes. Both 1,4-oxoiminations and 1,4-hydroxyiminations increase the molecular complexity of products.