1283073-99-3

Basic information

• Product Name: 2-(2,3-diphenyl-1H-indol-1-yl)quinoline
• CAS NO: 1283073-99-3
• Molecular Weight: 396.491
• Mol File: 1283073-99-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(2,3-diphenyl-1H-indol-1-yl)quinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,3-diphenyl-1H-indol-1-yl)quinoline(1283073-99-3)
• EPA Substance Registry System: 2-(2,3-diphenyl-1H-indol-1-yl)quinoline(1283073-99-3)

Safety Data

• Hazardous Substances Data: 1283073-99-3(Hazardous Substances Data)

Upstream product

• 5468-85-9 N-phenylquinolin-2-amine 
• 501-65-5 diphenyl acetylene 

Relevant articles and documents

Synthesis of N-(2-pyridyl)indoles via Pd(II)-catalyzed oxidative coupling

Readily available Pd(II) chloride catalysts can catalyze selective and efficient oxidative coupling between N-aryl-2-aminopyridines and internal alkynes to yield N-(2-pyridyl)indoles. This process involves the ortho C-H activation of N-aryl-2-aminopyridines, and CuCl2 was used as an oxidant. Compared to our previously reported Rh(III)-catalyzed synthesis of this class of product, this method is advantageous with a wider scope of alkynes and cost-effective Pd(II) catalysts. Molecular oxygen can be used as a terminal oxidant.