122041-25-2

Usage

Uses

Used in Polymer and Plastics Industry:
2,6-DIFLUORO-4'-METHYLBENZOPHENONE is used as a photoinitiator for [application reason] its ability to absorb light and initiate chemical reactions, which is crucial in the photopolymerization process. This application is vital for the production of various polymers and plastics, enhancing their properties and performance.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 2,6-DIFLUORO-4'-METHYLBENZOPHENONE is used as an intermediate in the synthesis of various pharmaceuticals. Its unique chemical properties contribute to the development of new drugs with improved efficacy and safety profiles.
Used in Agrochemical Synthesis:
Similarly, in the agrochemical sector, 2,6-DIFLUORO-4'-METHYLBENZOPHENONE is utilized as a key intermediate in the synthesis of agrochemicals. Its involvement in the production process helps create effective and environmentally friendly solutions for agricultural applications.

Upstream product

• 108-88-3 toluene 
• 385-00-2 2,6-difluorobenzoic acid 

Relevant academic research and scientific papers

Poly(ethylene glycol) dimethyl ether mediated oxidative scission of aromatic olefins to carbonyl compounds by molecular oxygen

A simple, and practical oxidative scission of aromatic olefins to carbonyl compounds using O2as the sole oxidant with poly(ethylene glycol) dimethyl ether as a benign solvent has been developed. A wide range of monosubstituted,gem-disubstituted, 1,2-disubstituted, trisubstituted and tetrasubstituted aromatic olefins was successfully converted into the corresponding aldehydes and ketones in excellent yields even with gram-scale reaction. Some control experiments were also conducted to support a possible reaction pathway.

Method for preparing aldehyde ketone compound through olefin oxidation

The invention provides a method for preparing an aldehyde ketone compound by olefin oxidation, which relates to an olefin oxidative cracking reaction in which oxygen participates. The method comprises the following specific steps: in the presence of a solvent and an oxidant, carrying out oxidative cracking on an olefin raw material to obtain a corresponding aldehyde ketone product. Compared with the traditional method, the method does not need to add any catalyst or ligand, does not need to use high-pressure oxygen, has the advantages of simple and mild reaction conditions, environment friendliness, low cost, high atom economy and the like, is wide in substrate application range and high in yield, and has a wide application prospect in the aspects of synthesis of aldehyde ketone medical intermediates and chemical raw materials.

Erbium trifluoromethanesulfonate catalyzed Friedel-Crafts acylation using aromatic carboxylic acids as acylating agents under monomode-microwave irradiation

Erbium trifluoromethanesulfonate is found to be a good catalyst for the Friedel-Crafts acylation of arenes containing electron-donating substituents using aromatic carboxylic acids as the acylating agents under microwave irradiation. An effective, rapid and waste-free method allows the preparation of a wide range of aryl ketones in good yields and in short reaction times with minimum amounts of waste.