213470-31-6

Basic information

• Product Name: Quinoline, 5-methoxy-2-phenyl-
• CAS NO: 213470-31-6
• Molecular Formula: C16H13NO
• Molecular Weight: 235.285
• Mol File: 213470-31-6.mol

Chemical Properties

• CAS DataBase Reference: Quinoline, 5-methoxy-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Quinoline, 5-methoxy-2-phenyl-(213470-31-6)
• EPA Substance Registry System: Quinoline, 5-methoxy-2-phenyl-(213470-31-6)

Safety Data

• Hazardous Substances Data: 213470-31-6(Hazardous Substances Data)

Upstream product

• 698984-30-4 2,2-dimethyl-N-{3-(methyloxy)-2-[(1E)-3-oxo-3-phenyl-1-propen-1-yl]phenyl}propanamide 
• 56619-93-3 N-(3-methoxyphenyl)pivalamide 

Downstream Products

• 698984-37-1 5-hydroxy-2-phenylquinoline 

Relevant articles and documents

BENZOXAZINONE DERIVATIVES, PREPARATION THEREOF AND USES IN THE TREATMENT OF CNS AND OTHER DISORDERS

Compounds of formula (I) and pharmaceutically acceptable salts thereof are disclosed:wherein A, R1, R2, R3, p, q, A and X are as defined in the specification. Preparation of the compounds and uses in the treatment of CNS and other disorders, including dep

Friedlaender Synthesis of Substituted Quinolines from N-Pivaloylanilines

Synthesis of a great variety of quinoline derivatives has been developed by lithiation of N-pivaloylanilines with sec-BuLi, formylation with DMF, and subsequent condensation with active methylene groups of aldehydes or ketones (KHMDS).The pivaloyloxy group is eliminated during one-pot procedure in most cases.The scope of the reaction has been studied, showing that the method is limited by the nature of intermediate compounds. - Keywords: Friedlaender synthesis; pivaloylanilines; quinolines; o-metalation; one-pot synthesis