1031928-45-6

Basic information

• Product Name: 7-METHYL-3-PHENYL-2-QUINOLINOL
• Synonyms: 7-METHYL-3-PHENYL-2-QUINOLINOL;2-Hydroxy-7-methyl-3-phenylquinoline
• CAS NO: 1031928-45-6
• Molecular Formula: C₁₆H₁₃NO
• Molecular Weight: 235.28052
• Mol File: 1031928-45-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 7-METHYL-3-PHENYL-2-QUINOLINOL(CAS DataBase Reference)
• NIST Chemistry Reference: 7-METHYL-3-PHENYL-2-QUINOLINOL(1031928-45-6)
• EPA Substance Registry System: 7-METHYL-3-PHENYL-2-QUINOLINOL(1031928-45-6)

Safety Data

• Hazardous Substances Data: 1031928-45-6(Hazardous Substances Data)

Upstream product

• 20357-22-6 2-nitro-4-methylbenzaldehyde 
• 100-44-7 benzyl chloride 
• 103-83-3 N,N'-dimethylbenzylamine 
• 100-52-7 benzaldehyde 
• 260783-80-0 N,N,N--trimethyl--1--phenylmethanaminium trifluoromethanesulfonate 
• 13939-06-5 molybdenum hexacarbonyl 
• 824-54-4 2-bromo-4-methylbenzaldehyde 
• 103-81-1 Benzeneacetamide 

Relevant articles and documents

Palladium-Catalyzed Reductive Aminocarbonylation of Benzylammonium Triflates with o-Nitrobenzaldehydes for the Synthesis of 3-Arylquinolin-2(1 H)-ones

A palladium-catalyzed straightforward procedure for the synthesis of 3-arylquinolin-2(1H)-ones has been developed. The synthesis proceeds through a palladium-catalyzed reductive aminocarbonylation reaction of benzylic ammonium triflates with o-nitrobenzaldehydes, and a wide range of 3-arylquinolin-2(1H)-ones was obtained in moderate to good yields with very good functional group compatibility.

Copper(I) iodide catalyzed synthesis of quinolinones via cascade reactions of 2-halobenzocarbonyls with 2-arylacetamides

An efficient copper-catalyzed method for the synthesis of quinolinones, pyridinones, and heteroannulated pyridinones via cascade reactions of substituted 2-iodo-, 2-bromo-, and 2-chlorobenzocarbonyls with 2-arylacetamides is reported. The protocol works well for the reaction of most of the 2-iodo-, 2-bromo- and 2-chlorobenzocarbonyls with 2-arylacetamides. Georg Thieme Verlag Stuttgart · New York.