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Usage

Uses

Used in Pharmaceutical Industry:
2',5'-DIMETHYL-3-PHENYLPROPIOPHENONE is used as a precursor in the synthesis of pharmaceuticals for its versatile chemical properties, contributing to the development of various medicinal compounds.
Used in Flavor and Fragrance Industry:
2',5'-DIMETHYL-3-PHENYLPROPIOPHENONE is used as a flavoring agent and fragrance ingredient due to its sweet, floral, and fruity aroma, enhancing the sensory qualities of various products.
Used in Dye Production:
2',5'-DIMETHYL-3-PHENYLPROPIOPHENONE is used as an intermediate in the production of dyes, playing a crucial role in the creation of colorants for different applications.
Used in Polymer Production:
2',5'-DIMETHYL-3-PHENYLPROPIOPHENONE is also used as an intermediate in the production of polymers, contributing to the development of various types of plastics and materials with specific properties.
Used in Organic Compounds Synthesis:
2',5'-DIMETHYL-3-PHENYLPROPIOPHENONE is utilized as an intermediate in the synthesis of other organic compounds, showcasing its versatility in the chemical industry.

InChI:InChI=1/C17H18O/c1-13-8-9-14(2)16(12-13)17(18)11-10-15-6-4-3-5-7-15/h3-9,12H,10-11H2,1-2H3

Upstream product

• 106-42-3 para-xylene 
• 501-52-0 3-Phenylpropionic acid 
• 22422-19-1 3-chloro-1-(2,5-dimethylphenyl)propan-1-one 
• 98-80-6 phenylboronic acid 
• 2142-73-6 1-(2,5-dimethylphenyl)-1-ethanone 
• 100-51-6 benzyl alcohol 

Relevant academic research and scientific papers

A nanoscale iron catalyst for heterogeneous direct: N - And C -alkylations of anilines and ketones using alcohols under hydrogen autotransfer conditions

Here, we report a commercially available nanoscale Fe catalyst for heterogeneous direct N- and C-alkylation reactions of anilines and methyl ketones with alcohols. A hydrogen autotransfer mechanism has been found to operate in these reactions by deuterium labelling studies. In addition, dehydrogenative quinoline synthesis has been demonstrated from amino benzyl alcohols and acetophenones.

Rhodium(I)-catalyzed arylation of β-chloro ketones and related derivatives through domino dehydrochlorination/conjugate addition

Highly efficient arylations of β-chloro ketones and their ester and amide derivatives were achieved by means of domino dehydrochlorination/Rh(I)- catalyzed conjugate addition. In situ generated vinyl ketones and their analogues were identified as the reaction intermediates. The present synthetic protocol provides a concise route to (chiral) β-aryl ketones, esters, and amides. Copyright

Organic Reactions Catalyzed by Solid Superacids. 5. Perfluorinated Sulfonic Acid Resin (Nafion-H) Catalyzed Intramolecular Friedel-Crafts Acylation

Nafion-H, a perfluorinated sulfonic acid resin, catalyzed the intramolecular Friedel-Crafts acylation of diarylalkane-2-carboxylic acids and arylalkanoic acids in refluxing p-xylene to provide cyclic ketones.The reactions were clean, and the water that was formed as a byproduct did not deactivate the catalyst.It was also found that the intramolecular acylation of the corresponding acid chlorides occurred under much milder reaction conditions.The mechanism of the reaction is discussed.