1610886-26-4

Basic information

• Product Name: (6-methoxy-2-(5'-methoxypyridin-2'-yl)benzo[b]thiophen-3-yl)(4-(2-(piperidin-1-yl)ethoxy)phenyl)methanone
• Synonyms: (6-methoxy-2-(5'-methoxypyridin-2'-yl)benzo[b]thiophen-3-yl)(4-(2-(piperidin-1-yl)ethoxy)phenyl)methanone
• CAS NO: 1610886-26-4
• Molecular Weight: 502.634
• Mol File: 1610886-26-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (6-methoxy-2-(5'-methoxypyridin-2'-yl)benzo[b]thiophen-3-yl)(4-(2-(piperidin-1-yl)ethoxy)phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (6-methoxy-2-(5'-methoxypyridin-2'-yl)benzo[b]thiophen-3-yl)(4-(2-(piperidin-1-yl)ethoxy)phenyl)methanone(1610886-26-4)
• EPA Substance Registry System: (6-methoxy-2-(5'-methoxypyridin-2'-yl)benzo[b]thiophen-3-yl)(4-(2-(piperidin-1-yl)ethoxy)phenyl)methanone(1610886-26-4)

Safety Data

• Hazardous Substances Data: 1610886-26-4(Hazardous Substances Data)

Upstream product

• 1610886-25-3 5-methoxy-2-(6-methoxybenzo[b]thiophen-2-yl)pyridine 
• 182133-35-3 6-methoxy-benzo[b]thiophen-2-yl boronic acid 
• 105170-27-2 2-bromo-5-methoxypyridine 
• 3040-44-6 1-piperidinoethanol 
• 201230-82-2 carbon monoxide 
• 1610886-00-4 (4-fluorophenyl)(6-methoxy-2-(5-methoxypyridin-2-yl)benzo[b]thiophen-3-yl)methanone 

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.