167763-99-7

Basic information

• Product Name: N-benzyl-7-methoxy-4-methylquinolin-2(1H)-one
• Synonyms: N-benzyl-7-methoxy-4-methylquinolin-2(1H)-one
• CAS NO: 167763-99-7
• Molecular Weight: 279.338
• Mol File: 167763-99-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-benzyl-7-methoxy-4-methylquinolin-2(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-7-methoxy-4-methylquinolin-2(1H)-one(167763-99-7)
• EPA Substance Registry System: N-benzyl-7-methoxy-4-methylquinolin-2(1H)-one(167763-99-7)

Safety Data

• Hazardous Substances Data: 167763-99-7(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 90811-55-5 N-benzyl-(3-methoxyaniline) 
• 536-90-3 m-Anisidine 
• 25233-47-0 N-(3'-methoxyphenyl)-3-oxobutanamide 
• 40053-37-0 4-methyl-7-methoxy-2(1H)-quinolinone 
• 100-39-0 benzyl bromide 

Relevant articles and documents

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

The invention provides novel compounds and compositions of Formulas I and II, as well as methods of using them. The compounds can be used, for example, to quantify an amount of double stranded DNA in a sample subjected to nucleic acid amplification, or fo