39070-93-4

Basic information

• Product Name: (4-methoxyphenyl)(2-methylnaphthalen-1-yl)methanone
• Synonyms: (4-methoxyphenyl)(2-methylnaphthalen-1-yl)methanone
• CAS NO: 39070-93-4
• Molecular Weight: 276.335
• Mol File: 39070-93-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (4-methoxyphenyl)(2-methylnaphthalen-1-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (4-methoxyphenyl)(2-methylnaphthalen-1-yl)methanone(39070-93-4)
• EPA Substance Registry System: (4-methoxyphenyl)(2-methylnaphthalen-1-yl)methanone(39070-93-4)

Safety Data

• Hazardous Substances Data: 39070-93-4(Hazardous Substances Data)

Upstream product

• 1415033-47-4 1-[3-(4-methoxyphenyl)-1H-isochromen-1-yl]propan-2-one 
• 176910-67-1 2-(4-methoxyphenylethynyl)benzaldehyde 
• 91-57-6 2-Methylnaphthalene 
• 2586-62-1 1-bromo-2-methylnaphtalene 
• 100-07-2 4-methoxy-benzoyl chloride 

Downstream Products

• 15894-60-7 (4-Hydroxy-3,5-diiodo-phenyl)-(2-methyl-naphthalen-1-yl)-methanone 
• 39105-33-4 (3,5-Dibromo-4-hydroxy-phenyl)-(2-methyl-naphthalen-1-yl)-methanone 
• 39070-86-5 1-p-Hydroxybenzoyl-2-methylnaphthalin 

Relevant articles and documents

Catalytic c-c cleavage/alkyne-carbonyl metathesis sequence of cyclobutanones

A ring-opening/alkyne-carbonyl metathesis sequence of alkyne-tethered cyclobutanones catalyzed by AgSbF6 is realized for the first time to furnish multisubstituted naphthyl ketones under mild conditions. A range of substrates decorated with various substituents at different positions were all well accommodated. Preliminary mechanistic studies show that silver salt acted as a Lewis acid to facilitate both C-C cleavage of the cyclobutanone moiety and the subsequent metathesis between C═O and CC bonds.

Gold-catalyzed cyclo-isomerization of 1,6-diyne-4-en-3-ols to form naphthyl ketone derivatives

We report a new efficient gold-catalyzed cyclization of 1,6-diyne-4-en-3-ols to give naphthyl ketone derivatives under ambient conditions. The value of this cyclization is reflected by its applicability to a wide range of alcohol substrates. The Royal Society of Chemistry.