1609939-34-5

Basic information

• Product Name: 2-methoxy-3-phenylisoquinolin-1(2H)-one
• Synonyms: 2-methoxy-3-phenylisoquinolin-1(2H)-one
• CAS NO: 1609939-34-5
• Molecular Weight: 251.285
• Mol File: 1609939-34-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-methoxy-3-phenylisoquinolin-1(2H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methoxy-3-phenylisoquinolin-1(2H)-one(1609939-34-5)
• EPA Substance Registry System: 2-methoxy-3-phenylisoquinolin-1(2H)-one(1609939-34-5)

Safety Data

• Hazardous Substances Data: 1609939-34-5(Hazardous Substances Data)

Upstream product

• 609-67-6 2-Iodobenzoyl chloride 
• 1225463-02-4 2-iodo-N-methoxybenzamide 
• 2446-51-7 N-methoxybenzamide 
• 20718-17-6 2-(dimethyl(oxo)-λ⁶-sulfaneylidene)-1-phenylethan-1-one 
• 20187-61-5 mesyloxyacetophenone 
• 7257-94-5 1-phenyl-2-(p-tolylsulfonyloxy)ethanone 
• 532-27-4 1-chloroacetophenone 
• 70-11-1 α-bromoacetophenone 

Downstream Products

• 7115-13-1 3-phenyl-2H-isoquinolin-1-one 

Relevant articles and documents

Access to divergent benzo-heterocycles: Via a catalyst-dependent strategy in the controllable cyclization of o -alkynyl- N -methoxyl-benzamides

A chemo- and regio-selectively controllable approach for construction of diverse benzo-heterocycles is established. A new strategy for using the ligand effect in gold catalysis to control the regioselectivity in the cyclization of o-alkynyl-N-methoxyl-benzamide is successfully achieved. Meanwhile, the chemoselectivity between nitrogen and oxygen nucleophiles is precisely switched by gold and platinum catalysts.

Rhodium(III)-catalyzed chemodivergent annulations between: N-methoxybenzamides and sulfoxonium ylides via C-H activation

Chemodivergent and redox-neutral annulations between N-methoxybenzamides and sulfoxonium ylides have been realized via Rh(iii)-catalyzed C-H activation. The sulfoxonium ylide acts as a carbene precursor, and coupling occurs under acid-controlled condition