1610885-95-4

Basic information

• Product Name: (4-fluorophenyl)(1-(pyridin-2-yl)-indol-2-yl)methanone
• Synonyms: (4-fluorophenyl)(1-(pyridin-2-yl)-indol-2-yl)methanone
• CAS NO: 1610885-95-4
• Molecular Weight: 316.334
• Mol File: 1610885-95-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (4-fluorophenyl)(1-(pyridin-2-yl)-indol-2-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (4-fluorophenyl)(1-(pyridin-2-yl)-indol-2-yl)methanone(1610885-95-4)
• EPA Substance Registry System: (4-fluorophenyl)(1-(pyridin-2-yl)-indol-2-yl)methanone(1610885-95-4)

Safety Data

• Hazardous Substances Data: 1610885-95-4(Hazardous Substances Data)

Upstream product

• 459-57-4 4-fluorobenzaldehyde 
• 3419-91-8 N-(2-pyridyl)indole 
• 352-34-1 4-fluoro-1-iodobenzene 
• 201230-82-2 carbon monoxide 

Relevant articles and documents

Palladium-catalyzed direct C2-and further C7-acylation of indoles with aldehydes

The palladium-catalyzed direct C2- and further C7-acylation of indoles with aldehydes have been developed. This method provides a convenient pathway toward a variety of mono- and diacylated indoles. The palladium-catalyzed direct C2- and further C7-acylat

Regioselective ruthenium-catalyzed carbonylative direct arylation of five-membered and condensed heterocycles

A ruthenium-catalyzed carbonylative Ci￡H bond arylation process for the three-component synthesis of complex aryl-(hetero)aryl ketones in an aqueous solution has been developed. By exploiting the ortho-activating effect of nitrogen-containing directing groups, a regioselective, successive twofold C(sp2)i￡C(sp2) bond formation has been achieved. This straightforward catalytic process provides access to versatile products prevalent in multiple bioactive compounds and supplies a valuable functional group for subsequent transformations. Ci￡ H bond functionalization: A ruthenium-catalyzed carbonylative Ci￡H bond arylation process for the three-component synthesis of complex aryl-(hetero)aryl ketones in an aqueous solution has been developed (see scheme). By exploiting the ortho-activating effect of nitrogen-containing directing groups, a regioselective, successive twofold C(sp2) i￡C(sp2) bond formation has been achieved.