1392144-95-4

Basic information

• Product Name: (1-benzyl-5-bromo-1H-indol-3-yl)(phenyl)methanone
• Synonyms: (1-benzyl-5-bromo-1H-indol-3-yl)(phenyl)methanone
• CAS NO: 1392144-95-4
• Molecular Weight: 390.279
• Mol File: 1392144-95-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (1-benzyl-5-bromo-1H-indol-3-yl)(phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (1-benzyl-5-bromo-1H-indol-3-yl)(phenyl)methanone(1392144-95-4)
• EPA Substance Registry System: (1-benzyl-5-bromo-1H-indol-3-yl)(phenyl)methanone(1392144-95-4)

Safety Data

• Hazardous Substances Data: 1392144-95-4(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 10075-50-0 5-bromo-1H-indole 
• 98-88-4 benzoyl chloride 
• 10075-51-1 1-benzyl-5-bromo-1H-indole 

Downstream Products

• 1410876-81-1 C₄₃H₃₁BrN₂O 
• 1410877-42-7 1-(1-benzyl-5-bromo-1H-indol-3-yl)-1,3-diphenylprop-2-yn-1-ol 

Relevant articles and documents

Palladium-Catalyzed 2-fold C-H Activation/C-C Coupling for C4-Arylation of Indoles Using Weak Chelation

Palladium-catalyzed weak chelation-assisted regioselective C4-arylation of indoles has been accomplished using a readily available arene at moderate temperature. The C4-arylation, weak chelating benzoyl (Bz) directing group, cross-dehydrogenative coupling (CDC), broad substrate scope, and late-stage diversifications are the important practical features.