107574-57-2

Usage

Compound type

ketone

Common uses

production of fragrances and flavors, fragrance ingredient in perfumes, soaps, and personal care products

Scent

sweet, floral

Aromatic properties

musky, woody note

Other uses

production of pharmaceuticals, synthesis of other organic compounds

Upstream product

• 93-08-3 methyl 2-naphthyl ketone 
• 67-56-1 methanol 
• 7228-47-9 2-(2-naphthyl)ethanol 
• 201230-82-2 carbon monoxide 
• 3857-83-8 2-naphthyl triflate 
• 1068-55-9 isopropylmagnesium chloride 

Downstream Products

• 93-09-4 naphthalene-2-carboxylate 
• 76636-01-6 2-methyl-1-(naphthalen-2-yl)propan-1-ol 
• 1069130-29-5 C₂₂H₁₈O 
• 1377585-46-0 N-[β-naptholoyl]-S-methyl-S-phenylsulfoximine 

Relevant academic research and scientific papers

Preparation and use of DMF-stabilized iridium nanoclusters as methylation catalysts using methanol as the C1 source

We report methylations of alcohols and anilines catalyzed by DMF-stabilized Ir nanoclusters using methanol as the C1 source. The DMF-stabilized Ir nanoclusters were prepared in one step and have diameters of 1-1.5 nm. They react in a borrowing-hydrogen reaction and are efficient methylation catalysts (TON up to 310?000).

Highly efficient Pd-catalyzed carbonylative cross-coupling reactions with tetraorganoindates

Tetraorganoindates, which were prepared easily from the reaction of 1 equiv of InCl3 with 4 equiv of organometallics, could be employed as effective nucleophilic cross-coupling partners in Pd-catalyzed carbonylative cross-coupling reactions with a variety of organic electrophiles. The present method gave unsymmetrical ketones and 1,4-diacylbenzenes in good yields with highly efficient transfer of almost all the organic groups attached to the indium under a carbon monoxide atmosphere in THF at 60 °C.