677302-48-6

Basic information

• Product Name: 1-benzenesulfonyl-1,4-dihydro-5H-pyrrolo[3,2-b]pyridin-5-one
• Synonyms: 1-benzenesulfonyl-1,4-dihydro-5H-pyrrolo[3,2-b]pyridin-5-one
• CAS NO: 677302-48-6
• Molecular Weight: 274.3
• Mol File: 677302-48-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-benzenesulfonyl-1,4-dihydro-5H-pyrrolo[3,2-b]pyridin-5-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzenesulfonyl-1,4-dihydro-5H-pyrrolo[3,2-b]pyridin-5-one(677302-48-6)
• EPA Substance Registry System: 1-benzenesulfonyl-1,4-dihydro-5H-pyrrolo[3,2-b]pyridin-5-one(677302-48-6)

Safety Data

• Hazardous Substances Data: 677302-48-6(Hazardous Substances Data)

Usage

Type of compound

Heterocyclic compound

Core structure

Pyrrolopyridine

Substituent

Benzenesulfonyl group

Potential applications

Biological activities, building block in pharmaceuticals and agrochemicals, material science, and organic chemistry

Precautions

May pose health hazards if not properly managed and stored.

Upstream product

• 17288-40-3 5-methoxy-4-aza-1H-indole 
• 111795-99-4 2-(6-methoxy-3-nitropyridin-2-yl)acetonitrile 
• 5446-92-4 2-methoxy-5-nitropyridine 
• 372077-49-1 1-benzenesulfonyl-5-methoxy-1H-pyrrolo[3,2-b]pyridine 

Downstream Products

• 737003-25-7 1-benzenesulfonyl-5-(4-bromobutoxy)-1H-pyrrolo[3,2-b]pyridine 
• 1206181-57-8 trifluoromethanesulfonic acid 1-benzenesulfonyl-1H-pyrrolo[3,2-b]pyridin-5-yl ester 
• 737003-33-7 1,6-bis[(1-benzenesulfonyl-1H-pyrrolo[3,2-b]pyridin-5-yl)oxy]hexane 
• 737003-32-6 1,5-bis[(1-benzenesulfonyl-1H-pyrrolo[3,2-b]pyridin-5-yl)oxy]pentane 
• 737003-31-5 1,4-bis[(1-benzenesulfonyl-1H-pyrrolo[3,2-b]pyridin-5-yl)oxy]butane 
• 737003-26-8 1-benzenesulfonyl-5-(5-bromopentyloxy)-1H-pyrrolo[3,2-b]pyridine 
• 737003-27-9 1-benzenesulfonyl-5-(6-bromohexyloxy)-1H-pyrrolo[3,2-b]pyridine 

Relevant articles and documents

Convenient access to C-2 or C-5 substituted 4-azaindole derivatives

Functionalization at C-2 and C-5 of N-benzenesulfonyl-4-azaindole 1 was performed by lithiation reactions and original palladium-catalyzed chemistry. It led to very useful new substituted 4-azaindole derivatives in fair to high yields.