708-66-7

Usage

Uses

Used in Pharmaceutical Industry:
4-(TRIFLUOROMETHYLSULFINYL)CHLOROBENZENE is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(TRIFLUOROMETHYLSULFINYL)CHLOROBENZENE is utilized as an intermediate in the production of agrochemicals, including insecticides and herbicides. Its properties make it a valuable asset in creating effective compounds for pest and weed control, thereby supporting agricultural productivity.
Used in Organic Chemistry:
4-(TRIFLUOROMETHYLSULFINYL)CHLOROBENZENE is used as a building block in organic chemistry for the manufacturing of a range of organic compounds. Its trifluoromethylsulfinyl group provides unique reactivity and selectivity in chemical reactions, facilitating the synthesis of complex organic molecules.

InChI:InChI=1/C7H4ClF3OS/c8-5-1-3-6(4-2-5)13(12)7(9,10)11/h1-4H

Upstream product

• 407-16-9 4-chlorophenyl trifluoromethyl sulfide 
• 108-90-7 chlorobenzene 
• 1948-15-8 <4-Chlor-2-nitro-phenyl>-trifluormethyl-sulfoxid 
• 1142-19-4 4,4'-dichlorodiphenyl disulfide 
• 2901-92-0 p-chlorophenylsulfinyl chloride 
• 81290-20-2 (trifluoromethyl)trimethylsilane 
• 1948-10-3 (2-Amino-4-chlor-phenyl)-trifluormethyl-sulfoxid 

Downstream Products

• 95970-28-8 C₈H₄ClF₆NO₂S₂ 
• 1178899-25-6 N-acetyl-S-(p-chlorophenyl)-S-(trifluoromethyl)sulfilimine 
• 1260111-72-5 p-chlorophenyl trifluoromethyl sulfilimine 
• 1335015-55-8 N-(phenyl) (p-chloro)phenyl trifluoromethyl sulfoximine 
• 95414-69-0 S-((p-chloro)phenyl)-S-(trifluoromethyl)-sulfoximine 

Relevant academic research and scientific papers

Selective oxidation and chlorination of trifluoromethylsulfide using trichloroisocyanuric acid in ionic liquid

A route to chemoselective oxidation and chlorination of aryltrifluoromethylsulfide using trichloroisocyanuric acid (TCCA) in ionic liquid, an efficiently O-methylation reaction and a reduction of nitro- to amido- in excellent yields have been developed.

Method for condensation of aromatic derivative(s) and a sulphinic derivative

The invention concerns a method for the condensation of aromatic derivative(s) or a sulphinic derivative by a perhalogenated, advantageously perfluorinated, carbon atom. Said method is characterized in that it consists in subjecting said sulphinic derivat

Nucleophilic trifluoromethylation of organic substrates using (trifluoromethyl)trimethylsilane in the presence of a fluoride anion. II. A convenient route to aryltrifluoromethyl-sulfides, - sulfoxides and -sulfones

Aryltrifluoromethyl-sulfides, -sulfoxides and -sulfones can be prepared by trifluoromethylation of the corresponding arylsulfenyl, -sulfinyl and -sulfonyl halides using (trifluoromethyl)trimethylsilane in the presence of fluoride sources, such as TASF . - Keywords: Nucleophilic trifluoromethylation; (Trifluoromethyl)trimethylsilane; Fluoride anion; Aryltrifluoromethylsulfides; Aryltrifluoromethylsulfoxides; Aryltrifluoromethylsulfones

FLUORO(TRIFLUOROMETHYL)ARYLSULFONIUM AND (TRIFLUOROMETHYL)DIARYLSULFONIUM SALTS

The oxygen atoms in aryl trifluoromethyl sulfoxides are substituted by fluorine during the action of the SF3(1+)*BF4(1-) and SF3(1+)*SbF6(1-) complexes.Fluoro(trifluoromethyl)arylsulfonium and (trifluoromethyl)diarylsulfonium salts were synthesized.The la