20915-78-0

Basic information

• Product Name: 6-methoxy-1-phenyl-3,4-dihydronaphthalen-2(1H)-one
• Synonyms: 6-methoxy-1-phenyl-3,4-dihydronaphthalen-2(1H)-one
• CAS NO: 20915-78-0
• Molecular Weight: 252.313
• Mol File: 20915-78-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6-methoxy-1-phenyl-3,4-dihydronaphthalen-2(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 6-methoxy-1-phenyl-3,4-dihydronaphthalen-2(1H)-one(20915-78-0)
• EPA Substance Registry System: 6-methoxy-1-phenyl-3,4-dihydronaphthalen-2(1H)-one(20915-78-0)

Safety Data

• Hazardous Substances Data: 20915-78-0(Hazardous Substances Data)

Upstream product

• 2844-82-8 methoxy-6, phenyl-1, dihydro-3,4 naphtalene 

Relevant articles and documents

Oxone-acetone mediated Wacker-type oxidation of benzo-fused olefins

Herein we disclose a novel application of the oxone-acetone combination for the Wacker-type oxidation of indenes and dihydronaphthalenes leading, respectively, to indan-2-ones and 2-tetralones. The amount of the base employed in the reaction seems to switch the reaction path from dioxygenation to Wacker-type oxidation. Control experiments suggest that the reaction is not proceeding via the epoxide route and also that there is no role of trace amounts of metals present in the reagents on the current oxidation.

Hydroborations: A new route for the preparation of 1-alkyl- (or aryl) 2-tetralones

The hydroboration followed by chromic acid oxidation of 1-alkyl- and 1-aryl-3,4-dihydronaphthalenes leads to the corresponding 1-alkyl- (or aryl)2-tetralones (1-substituted 3,4-dihydronaphthalen-2(1H)-ones.