74803-15-9

Basic information

• Product Name: 2,3-diphenyl-1H-pyrrolo[2,3-b]pyridine
• Synonyms: 2,3-diphenyl-1H-pyrrolo[2,3-b]pyridine
• CAS NO: 74803-15-9
• Molecular Weight: 270.334
• Mol File: 74803-15-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,3-diphenyl-1H-pyrrolo[2,3-b]pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-diphenyl-1H-pyrrolo[2,3-b]pyridine(74803-15-9)
• EPA Substance Registry System: 2,3-diphenyl-1H-pyrrolo[2,3-b]pyridine(74803-15-9)

Safety Data

• Hazardous Substances Data: 74803-15-9(Hazardous Substances Data)

Upstream product

• 1160-81-2 (E)-2-(2-(1,2-diphenylethylidene)hydrazineyl)pyridine 
• 86119-84-8 phosphoric acid 
• 49609-84-9 2-Chloronicotinoyl chloride 
• 111108-72-6 (2-chloro-3-pyridinyl)methyl bromide 
• 42330-59-6 (2-chloropyrid-3-yl)methanol 
• 2942-59-8 2-chloronicotinic acid 
• 451-40-1 phenyl benzyl ketone 

Downstream Products

• 74803-18-2 3-benzoyl-2-(N-methylbenzoylamino)pyridine 1-oxide 
• 74803-19-3 3-benzoyl-2-(N-methylbenzoylamino)pyridine 
• 74803-17-1 7-methyl-2,3-diphenyl-7H-pyrrolo<2,3-b>pyridine 
• 74803-16-0 1-methyl-2,3-diphenyl-1H-pyrrolo<2,3-b>pyridine 

Relevant articles and documents

Iron-Catalyzed Radical Activation Mechanism for Denitrogenative Rearrangement Over C(sp3)–H Amination

An iron-catalyzed denitrogenative rearrangement of 1,2,3,4-tetrazole is developed over the competitive C(sp3)–H amination. This catalytic rearrangement reaction follows an unprecedented metalloradical activation mechanism. Employing the developed method, a wide number of complex-N-heterocyclic product classes have been accessed. The synthetic utility of this radical activation method is showcased with the short synthesis of a bioactive molecule. Collectively, this discovery underlines the progress of radical activation strategy that should find wide application in the perspective of medicinal chemistry, drug discovery and natural product synthesis research.