143301-49-9

Usage

Uses

Used in Flavoring and Fragrance Industry:
Ethanone, 2-(2,4-dimethylphenyl)-1-phenylis used as a flavoring and fragrance agent for its sweet, floral-like scent. It imparts a pleasant aroma to various products, enhancing their sensory appeal.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Ethanone, 2-(2,4-dimethylphenyl)-1-phenylis utilized as an intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Chemical Industry:
Ethanone, 2-(2,4-dimethylphenyl)-1-phenylis employed in the chemical industry for the production of resins, polymers, and other organic compounds. Its versatility as a chemical intermediate enables the creation of a wide range of products with diverse applications.
Used in Consumer Product Production:
Ethanone, 2-(2,4-dimethylphenyl)-1-phenylis used in the production of various consumer products, including cosmetics, personal care items, and household products. Its incorporation into these products enhances their sensory qualities and contributes to their overall performance.

Upstream product

• 7446-70-0 aluminium trichloride 
• 532-27-4 1-chloroacetophenone 
• 108-38-3 m-xylene 
• 473-72-3 (1'R,3'R)-2-(3'-acetyl-2',2'-dimethylcyclobutyl)acetic acid 
• 6331-04-0 2,4-dimethylphenylacetic acid 
• 90705-86-5 (2,4-dimethyl-phenyl)-acetyl chloride 
• 71-43-2 benzene 
• 28557-00-8 phenylzinc chloride 
• 68429-53-8 (2,4-dimethylphenyl)acetonitrile 
• 98-86-2 acetophenone 
• 576-22-7 2-Bromo-m-xylene 
• 94002-16-1 2,4-dimethylphenyl 4-methylbenzenesulfonate 
• 17879-35-5 cis-pinonic acid 

Downstream Products

• 24942-82-3 trans-1-phenyl-2-(2',4'-dimethylphenyl)-ethylene 
• 854224-97-8 (+/-)-α'-hydroxy-2.4-dimethyl-bibenzyl 

Relevant academic research and scientific papers

Thianthrenation-enabled α-arylation of carbonyl compounds with arenes

The Pd-catalyzed α-arylation of carbonyl compounds with simple arenes enabled by site-selective thianthrenation has been demonstrated. This onepot process using thianthrenium salts as the traceless arylating reagents features mild conditions and a broad substrate scope. In addition, this protocol could also tolerate the heterocyclic carbonyl compounds and complex bioactive molecules, which is appealing for medicinal chemistry.

Novel bisamide palladium(II) pincer complexes: effective catalysts in α-arylation of ketones

Three benzenedicarboxamide ligands (L) were designed and synthesized, and each was used to prepare a palladium(II) complex Pd(L)Br and Pd(L)(OAc). These NCN pincer complexes were used to catalyze the α-arylations of a variety of ketones with aryl chlorides or bromides in various solvents, and moderate-to-excellent yields were obtained (up to 95%). Further research showed that unactivated and sterically hindered aryl halides and ketones are also suitable substrates for the synthesis of α-arylation. Graphical Abstract: [Figure not available: see fulltext.].

Exploiting Aryl Mesylates and Tosylates in Catalytic Mono-α-arylation of Aryl- and Heteroarylketones

The first general palladium catalyst for the catalytic mono-α-arylation of aryl- and heteroarylketones with aryl mesylates and tosylates is described. The newly developed indolyl-derived phosphine ligand L7 has been identified to promote this reaction eff