1361029-49-3

Basic information

• Product Name: (E)-2-methyl-1-(3-methyl-1H-indol-1-yl)-3-(4-nitrophenyl)prop-2-en-1-one
• Synonyms: (E)-2-methyl-1-(3-methyl-1H-indol-1-yl)-3-(4-nitrophenyl)prop-2-en-1-one
• CAS NO: 1361029-49-3
• Molecular Weight: 320.348
• Mol File: 1361029-49-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-2-methyl-1-(3-methyl-1H-indol-1-yl)-3-(4-nitrophenyl)prop-2-en-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-methyl-1-(3-methyl-1H-indol-1-yl)-3-(4-nitrophenyl)prop-2-en-1-one(1361029-49-3)
• EPA Substance Registry System: (E)-2-methyl-1-(3-methyl-1H-indol-1-yl)-3-(4-nitrophenyl)prop-2-en-1-one(1361029-49-3)

Safety Data

• Hazardous Substances Data: 1361029-49-3(Hazardous Substances Data)

Upstream product

• 555-16-8 4-nitrobenzaldehdye 
• 13048-77-6 (E)-2-methyl-3-(4-nitrophenyl)acrylic acid 

Downstream Products

• 1361029-59-5 2,9-dimethyl-1-(4-nitrophenyl)-3H-pyrrolo[1,2-a]indol-3-one 

Relevant articles and documents

Aerobic palladium(II)-catalyzed 5-endo-trig cyclization: An entry into the diastereoselective C-2 alkenylation of indoles with tri- and tetrasubstituted double bonds

The endo trick: An endo ring closure onto the trigonal β carbon atom of α,β-unsaturated acceptors that are tethered to the indole nitrogen atom followed by amide cleavage enables the diastereoselective C-2 alkenylation of indoles with fully substituted double bonds. The carboxy group functions as a synthetically useful temporary tether (see scheme). Copyright