1644275-20-6

Basic information

• Product Name: methyl (1-methyl-4-oxo-2-phenyl-4,5,6,7-tetrahydro-1H-indol-3-yl)-acetate
• Synonyms: methyl (1-methyl-4-oxo-2-phenyl-4,5,6,7-tetrahydro-1H-indol-3-yl)-acetate
• CAS NO: 1644275-20-6
• Molecular Weight: 297.354
• Mol File: 1644275-20-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl (1-methyl-4-oxo-2-phenyl-4,5,6,7-tetrahydro-1H-indol-3-yl)-acetate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (1-methyl-4-oxo-2-phenyl-4,5,6,7-tetrahydro-1H-indol-3-yl)-acetate(1644275-20-6)
• EPA Substance Registry System: methyl (1-methyl-4-oxo-2-phenyl-4,5,6,7-tetrahydro-1H-indol-3-yl)-acetate(1644275-20-6)

Safety Data

• Hazardous Substances Data: 1644275-20-6(Hazardous Substances Data)

Upstream product

• 1075-06-5 2,2-dihydroxy-1-phenyl-ethanone 
• 55998-74-8 3-(methylamino)-2-cyclohexen-1-one 
• 67-56-1 methanol 
• 1651177-18-2 C₁₇H₁₇NO₃ 
• 1628708-23-5 2-cyano-2-(1-methyl-4-oxo-2-phenyl-4,5,6,7-tetrahydro-1H-3-indolyl)acetamide 

Downstream Products

• 1644275-30-8 methyl (4-hydroxy-1-methyl-2-phenylindol-3-yl)acetate 

Relevant articles and documents

Substituted benzo[a]carbazoles and indoleacetic acids from arylglyoxals and enamines through domino condensation, thermal cyclization, and aromatization

A two-step method has been developed in which cyclohexanone-fused 2-(3-pyrrolyl)-2-cyanoacetamides, the condensation products of enamines, arylglyoxals, and malononitrile, are converted into highly substituted benzo[a]carbazoles through a one-step thermal cyclization and palladium-catalyzed aromatization. The biologically important indoleacetic acid derivatives are also obtained in good yields from the hydrolysis and aromatization of the same cyanoacetamides. Copyright