117839-37-9

Basic information

• Product Name: 6-methoxy-2-(p-tolyl)quinoline
• Synonyms: 6-methoxy-2-(p-tolyl)quinoline
• CAS NO: 117839-37-9
• Molecular Weight: 249.312
• Mol File: 117839-37-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 6-methoxy-2-(p-tolyl)quinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 6-methoxy-2-(p-tolyl)quinoline(117839-37-9)
• EPA Substance Registry System: 6-methoxy-2-(p-tolyl)quinoline(117839-37-9)

Safety Data

• Hazardous Substances Data: 117839-37-9(Hazardous Substances Data)

Upstream product

• 5263-87-6 6-methoxy quinoline 
• 98-59-9 p-toluenesulfonyl chloride 
• 79-24-3 Nitroethane 
• 104-87-0 4-methyl-benzaldehyde 
• 104-94-9 4-methoxy-aniline 
• 84666-26-2 (6-Methoxy-2-p-tolyl-quinolin-4-yl)-methanesulfonyl chloride 
• 84666-27-3 2-(p-tolyl)-6-methoxy-4-quinolinemethanol 
• 18193-09-4 2-(p-tolyl)-6-methoxy-4-quinolinecarboxylic acid 

Relevant articles and documents

Synergy of anodic oxidation and cathodic reduction leads to electrochemical deoxygenative C2 arylation of quinoline: N-oxides

The first example of electrochemical deoxygenative C2 arylation of quinoline N-oxides using sulfonyl hydrazines was demonstrated in this work. By employing both anodic oxidation and cathodic reduction, a variety of 2-arylquinolines were synthesized under metal catalyst-, exogenous-oxidant-, and exogenous-reductant-free conditions.

The Role of Exciplexes in the Photoreduction of Quinolinemethanols

The photoreduction of a family of quinolinemethanols has been examined both in the presence and absence of exciplex-forming additives.Photoreduction of the alcohol group and cleavage of the side chain occurs on direct photolysis.However, irradiation with triethylamine led to predominant cleavage of the side chain while irradiation with 1,3-dicyanobenzene predominantly led to photoreduction of the alcohol functionality.A variety of other experiments supported the involvement of exciplexes in these transformations.