698975-01-8

Basic information

• Product Name: 4-chloro-N-(quinolin-2-yl)benzamide
• Synonyms: 4-chloro-N-(quinolin-2-yl)benzamide
• CAS NO: 698975-01-8
• Molecular Weight: 282.729
• Mol File: 698975-01-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-chloro-N-(quinolin-2-yl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chloro-N-(quinolin-2-yl)benzamide(698975-01-8)
• EPA Substance Registry System: 4-chloro-N-(quinolin-2-yl)benzamide(698975-01-8)

Safety Data

• Hazardous Substances Data: 698975-01-8(Hazardous Substances Data)

Upstream product

• 103802-43-3 2-(4-chlorophenyl)imidazo[1,2-a]quinoline 
• 606-43-9 1-methyl-2-quinolin-2(1H)-one 
• 619-56-7 4-chlorobenzamide 
• 1878-66-6 4-chlorophenylacetic Acid 
• 580-22-3 2-aminoquinoline 
• 623-03-0 4-Cyanochlorobenzene 
• 1613-37-2 Quinoline N-oxide 

Relevant articles and documents

Singlet oxygen mediated dual C-C and C-N bond cleavage in visible light

A tandem cleavage of carbon-carbon and carbon-nitrogen bonds in imidazo[1,2-a]pyridines and imidazo[1,2-a]quinolines is reported in the presence of eosin Y and visible light. The ring opening occurs under ambient conditions through singlet oxygen insertio

Copper(II)-mediated, carbon degradation-based amidation of phenylacetic acids toward N -substituted benzamides

The unprecedented synthesis of N-aryl substituted benzamides via the assembly of primary amines and phenylacetic acids has been developed in the presence of copper(ii) acetate. This tandem transformation involving carbon-carbon bond cleavage provides a complementary tool with particular application in the synthesis of secondary benzamides.