61304-90-3

Basic information

• Product Name: 2(1H)-Quinolinone, 7-methoxy-4-methyl-1-phenyl-
• CAS NO: 61304-90-3
• Molecular Formula: C17H15NO2
• Molecular Weight: 265.312
• Mol File: 61304-90-3.mol

Chemical Properties

• CAS DataBase Reference: 2(1H)-Quinolinone, 7-methoxy-4-methyl-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(1H)-Quinolinone, 7-methoxy-4-methyl-1-phenyl-(61304-90-3)
• EPA Substance Registry System: 2(1H)-Quinolinone, 7-methoxy-4-methyl-1-phenyl-(61304-90-3)

Safety Data

• Hazardous Substances Data: 61304-90-3(Hazardous Substances Data)

Upstream product

• 2540-30-9 1,2-dihydro-4-methyl-1-phenyl-2-quinolone 
• 55514-14-2 3-methyl-2-(methylthio)benzothiazolium tosylate 
• 591-50-4 iodobenzene 
• 40053-37-0 4-methyl-7-methoxy-2(1H)-quinolinone 
• 127-19-5 N,N-dimethyl acetamide 
• 12775-96-1 copper 
• 536-90-3 m-Anisidine 
• 25233-47-0 N-(3'-methoxyphenyl)-3-oxobutanamide 

Relevant articles and documents

Visible-Light-Photocatalyzed Synthesis of Phenanthridinones and Quinolinones via Direct Oxidative C-H Amidation

A straightforward synthetic strategy to construct biologically relevant phenanthridinones and quinolinones was developed via visible-light-promoted direct oxidative C-H amidation. In this photocatalytic system, amidyl radicals can be generated by homolysis of the N-H bond of simple amide precursors via single-electron transfer under blue LED illumination, which leads to oxidative intramolecular C-H amidation. Moreover, an efficient synthetic strategy using a photocascade enabled facile assembly of quinolinone structures through a catalytic sequence involving triplet energy (ET) transfer-based E/Z olefin isomerization and subsequent photocatalytic generation of amidyl radical intermediates.

Gold-Catalyzed Hydroarylation of N-Aryl Alkynamides for the Synthesis of 2-Quinolinones

A mild method for the synthesis of 2-quinolinones via hydroarylation of N-aryl alkynamides is reported. While traditional methods have relied on the use of strong Br?nsted or Lewis acids, this report describes the development of mild reaction conditions that yield 2-quinolinones in good to excellent yield using a commercially available gold catalyst. Substrates bearing a variety of functional groups are presented, with N-substitution proving to be key to the reactivity of several substrates.

Nucleic acid binding dyes and uses therefor

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NUCLEIC ACID BINDING DYES AND USES THEREFOR

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