56964-63-7

Usage

Uses

Used in the Chemical Industry:
2,4-Dibenzyl-3-pentanone is utilized as a solvent in various industrial applications, leveraging its ability to dissolve a wide range of substances, which is crucial for processes such as manufacturing and formulation.
Used in the Flavor and Fragrance Industry:
It serves as a flavoring agent and fragrance ingredient, contributing to the creation of perfumes and other personal care products. Its mild, sweet odor makes it a valuable component in these formulations.
Used in the Pharmaceutical Industry:
2,4-Dibenzyl-3-pentanone is employed as an intermediate in the synthesis of various drugs and pharmaceutical compounds. Its role in the production process is essential for developing new medications and enhancing existing ones.
Used in the Production of Perfumes and Personal Care Products:
In this application industry, 2,4-Dibenzyl-3-pentanone is used as a fragrance ingredient for its mild, sweet scent, enhancing the sensory experience of the final products.

InChI:InChI=1/C19H22O/c1-15(13-17-9-5-3-6-10-17)19(20)16(2)14-18-11-7-4-8-12-18/h3-12,15-16H,13-14H2,1-2H3

Upstream product

• 29393-16-6 methyl 2-methyl-3-phenylpropionate 
• 67-56-1 methanol 
• 2550-26-7 4-Phenyl-2-butanone 
• 100-51-6 benzyl alcohol 
• 5396-91-8 1,5-diphenyl-3-pentanone 
• 42124-16-3 1,5-diphenyl-2,4-dimethyl-1,4-pentadien-3-one 

Relevant academic research and scientific papers

Syndiotactic Poly(aminostyrene)-Supported Palladium Catalyst for Ketone Methylation with Methanol

Palladium nanoparticles immobilized on an amino-functionalized syndiotactic polystyrene (sPS-N) served as a novel recyclable catalyst for the dimethylation and cross methyl alkylation of a wide range of ketones with methanol as the methylation agent. This heterogeneous catalyst (Pd@sPS-N) was highly robust and showed excellent thermal stability and chemical resistance. It not only showed remarkably high activity, but it could also be easily recovered by filtration without loss of activity.

Rhodium-catalyzed ketone methylation using methanol under mild conditions: Formation of α-branched products

The rhodium-catalyzed methylation of ketones has been accomplished using methanol as the methylating agent and the hydrogen-borrowing method. The sequence is notable for the relatively low temperatures that are required and for the ability of the reaction system to form α-branched products with ease. Doubly alkylated ketones can be prepared from methyl ketones and two different alcohols by using a sequential one-pot iridium- and rhodium-catalyzed process. Uniquely effective for making branched alkyl products from ketones (see scheme): The scope of the presented reaction includes aromatic and aliphatic ketones and consecutive one-pot double alkylation reactions to provide a convenient route to branched ketones from simple methyl ketones. A brief study into the mechanism of the reaction has given evidence for an aldol-based reaction pathway.