1400791-58-3

Basic information

• Product Name: N-(2-(7-methyl-1H-indol-3-yl)ethyl)-N-(1-phenylallyl)acrylamide
• Synonyms: N-(2-(7-methyl-1H-indol-3-yl)ethyl)-N-(1-phenylallyl)acrylamide
• CAS NO: 1400791-58-3
• Molecular Weight: 344.456
• Mol File: 1400791-58-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-(2-(7-methyl-1H-indol-3-yl)ethyl)-N-(1-phenylallyl)acrylamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-(7-methyl-1H-indol-3-yl)ethyl)-N-(1-phenylallyl)acrylamide(1400791-58-3)
• EPA Substance Registry System: N-(2-(7-methyl-1H-indol-3-yl)ethyl)-N-(1-phenylallyl)acrylamide(1400791-58-3)

Safety Data

• Hazardous Substances Data: 1400791-58-3(Hazardous Substances Data)

Upstream product

• 14490-05-2 7-methyltryptamine 
• 85217-69-2 cinnamyl methyl carbonate 
• 1400791-77-6 N-(2-(7-methyl-1H-indol-3-yl)ethyl)-1-phenylprop-2-en-1-amine 
• 814-68-6 acryloyl chloride 

Downstream Products

• 1400791-40-3 (R)-10-methyl-11b-phenyl-5,6,11,11b-tetrahydro-1H-indolizino[8,7-b]indol-3(2H)-one 

Relevant articles and documents

Ring-closing metathesis/isomerization/pictet-spengler cascade via ruthenium/chiral phosphoric acid sequential catalysis

Chiral phosphoric acid worked together with Hoveyda-Grubbs II catalyst enabling highly efficient synthesis of enantioenriched tetrahydro-β- carbolines (up to 98% yield, 99% ee) through a ring-closing metathesis/ isomerization/Pictet-Spengler cascade reaction via sequential catalysis.