1644275-33-1

Basic information

• Product Name: methyl [1-benzyl-2-(4-fluorophenyl)-4-hydroxyindol-3-yl]acetate
• CAS NO: 1644275-33-1
• Molecular Weight: 389.426
• Mol File: 1644275-33-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl [1-benzyl-2-(4-fluorophenyl)-4-hydroxyindol-3-yl]acetate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl [1-benzyl-2-(4-fluorophenyl)-4-hydroxyindol-3-yl]acetate(1644275-33-1)
• EPA Substance Registry System: methyl [1-benzyl-2-(4-fluorophenyl)-4-hydroxyindol-3-yl]acetate(1644275-33-1)

Safety Data

• Hazardous Substances Data: 1644275-33-1(Hazardous Substances Data)

Upstream product

• 1651177-22-8 C₂₃H₂₀FNO₃ 
• 41609-04-5 N-benzyl-3-amino-2-cyclohexen-1-one 
• 1644275-24-0 methyl [1-benzyl-2-(4-fluorophenyl)-4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl]acetate 
• 1644275-40-0 2-[1-benzyl-2-(4-fluorophenyl)-4-oxo-4,5,6,7-tetrahydro-1H-3-indolyl]-2-cyanoacetamide 
• 447-43-8 1-(4-fluorophenyl)-2,2-dihydroxyethan-1-one 

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