1610885-85-2

Basic information

• Product Name: (2-(pyridin-2-yl)benzofuran-3-yl)(o-tolyl)methanone
• Synonyms: (2-(pyridin-2-yl)benzofuran-3-yl)(o-tolyl)methanone
• CAS NO: 1610885-85-2
• Molecular Weight: 313.356
• Mol File: 1610885-85-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2-(pyridin-2-yl)benzofuran-3-yl)(o-tolyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2-(pyridin-2-yl)benzofuran-3-yl)(o-tolyl)methanone(1610885-85-2)
• EPA Substance Registry System: (2-(pyridin-2-yl)benzofuran-3-yl)(o-tolyl)methanone(1610885-85-2)

Safety Data

• Hazardous Substances Data: 1610885-85-2(Hazardous Substances Data)

Upstream product

• 615-37-2 ortho-methylphenyl iodide 
• 201230-82-2 carbon monoxide 
• 7035-05-4 2-(benzofuran-2-yl)pyridine 
• 109-04-6 2-bromo-pyridine 
• 98437-24-2 benzofuran-2-boronic acid 

Relevant articles and documents

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.