930836-30-9

Usage

Uses

Used in Pharmaceutical Industry:
Chlorodifluoromethyl phenyl sulfone is utilized as a key intermediate in the synthesis of a variety of pharmaceuticals. Its unique chemical structure allows it to be a crucial component in the development of new drugs, contributing to advancements in medicinal chemistry.
Used in Agrochemical Industry:
ChlorodifluoroMethyl phenyl sulfone also plays a significant role in the agrochemical sector, where it is employed as an intermediate in the production of various agrochemicals. Its properties make it suitable for enhancing the effectiveness of pesticides and insecticides, thereby supporting agricultural productivity.
Used in Specialty Chemicals Production:
Chlorodifluoromethyl phenyl sulfone is used as a vital intermediate in the creation of specialty chemicals, which are essential for numerous applications, including the formulation of high-performance materials and the development of innovative products.
Used in Pesticide and Insecticide Development:
Due to its strong activity against certain pest species, chlorodifluoromethyl phenyl sulfone has been investigated for its potential use in the development of pesticides and insecticides, offering a promising avenue for improving pest control strategies.
Used in Material Science and Advanced Technologies:
ChlorodifluoroMethyl phenyl sulfone has been studied for its potential applications in material science, where it may contribute to the development of new materials with unique properties. Additionally, its exploration in advanced technologies suggests that it could play a role in the innovation of future technologies, expanding its impact across various fields.

Upstream product

• 701-65-5 (trichloromethylthio)benzene 
• 1535-65-5 difluoromethyl phenyl sulfone 
• 536975-50-5 [difluoro(phenylsulfonyl)methyl](trimethyl)silane 
• 80351-58-2 [(bromodifluoromethyl)sulfonyl]benzene 

Downstream Products

• 1004112-68-8 2-(3-chloro-5-(difluoromethoxy)phenyl)-1,3-dioxolane 
• 220173-84-2 1-(difluoromethyl)-2-phenyl-1H-imidazole 
• 1544-86-1 1-difluoromethoxy-4-nitrobenzene 
• 1004112-65-5 2-(difluoromethyl)-1-phenylpyrazolidin-3-one 
• 5905-69-1 1-bromo-4-(difluoromethoxy)benzene 
• 920981-10-8 1-(difluoromethoxy)naphthalene 
• 930836-31-0 1-(tert-butyl)-4-(difluoromethoxy)benzene 
• 128140-82-9 1-(difluoromethoxy)-4-iodobenzene 
• 175838-98-9 4-(difluoromethoxy)-1,1′-biphenyl 
• 1004112-64-4 4-benzoyl-2-(difluoromethyl)-3-methyl-1-phenyl-1,2-dihydropyrazol-5-one 
• 1004112-67-7 1-bromo-3-chloro-5-(difluoromethoxy)benzene 
• 81932-03-8 4-chloro-α,α-difluoroanisole 
• 772-23-6 2,4-di-chloro-1-(difluoromethoxy)benzene 
• 22225-77-0 1-difluoromethoxy-2-nitro-benzene 

Relevant academic research and scientific papers

A simple and efficient synthesis of trihalomethyl and dihalonitromethyl aryl sulfones

A method for the preparation of aryl trihalomethyl sulfones - active biocidal agents - with identical or different halogens is presented. The synthesis is based on the reaction of aryl methyl, aryl halomethyl, or aryl nitromethyl sulfones with sodium hypohalite. The method is simple in implementation, does not necessarily require the use of organic solvents, and selectively affords the products in good to excellent yields. Notably, it allows the preparation of the hitherto unknown phenyl trihalomethyl sulfone with three different halogens: fluorine, chlorine, and bromine.

Copper-mediated fluoroalkylation reactions with [(phenylsulfonyl)- difluoromethyl]trimethylsilane: Synthesis of PhSO2CF 2-containing allenes and alkynes

Copper-mediated (phenylsulfonyl)difluoromethylation of propargyl chlorides and alkynyl halides with PhSO2CF2TMS reagent was successfully achieved to give PhSO2CF2-containing allenes and alkynes, respectively. It is believed that the in situ formed PhSO 2CF2Cu species is involved in the present (phenylsulfonyl)difluoromethylation reactions. Georg Thieme Verlag Stuttgart · New York.

Chlorodifluoromethyl phenyl sulfone: A novel non-ozone-depleting substance-based difluorocarbene reagent for O- and N-difluoromethylations

Chlorodifluoromethyl phenyl sulfone, a previously unknown compound that can be readily prepared from non-ODS-based precursors, was found to act as a robust difluorocarbene reagent for O- and N-difluoromethylations. The Royal Society of Chemistry.