14055-48-2

Usage

Type of compound

Fluorinated aromatic compound

Structure

Contains both fluorine and benzene rings

Common uses

a. Production of specialty chemicals
b. Pharmaceuticals
c. Agrochemicals

Known for

a. High stability
b. Inertness

Industrial applications

Useful for various applications due to its stability and inertness

Unique structure and properties

Makes it a valuable building block for synthesizing other fluorine-containing compounds

Role in organic chemistry

Plays a crucial role in the field of organic chemistry

Development of advanced materials

Key component in the development of advanced materials and substances

Upstream product

• 363-72-4 Pentafluorobenzene 
• 2263-53-8 sodium pentafluorophenolate 
• 135736-89-9 C₁₂F₉IO 
• 14055-44-8 4-bromo-perfluorodiphenylether 
• 344-07-0 1-chloro-2,3,4,5,6-pentafluorobenzene 
• 186581-53-3 diazomethane 
• 17540-45-3 4-pentafluorophenoxy-2,3,4,5,6-pentafluorocyclohexa-2,5-dienone 
• 879-06-1 pentafluorophenylmagnesium chloride 
• 832-53-1 pentafluorobenzenesulonyl chloride 
• 827-15-6 1,2,3,4,5-pentafluoro-6-iodobenzene 
• 140200-31-3 2,3,4,5,6-Pentafluoro-benzenesulfonic acid pentafluorophenyl ester 

Downstream Products

• 20546-10-5 4-lithium perfluoro diphenylether 

Relevant academic research and scientific papers

Acid-catalyzed polyfluoroarylation of arenes with polyfluorinated mono- and tris(phenoxy)-1-oxaspiro[2.5]octa-4,7-dienes

4,5,6,7,8-Pentafluoro-6-pentafluorophenoxy-1-oxaspiro[2.5]octa-4,7-diene and 4,6,8-tri-fluoro-5,6,7-tris(pentafluorophenoxy)-1-oxaspiro[2.5]octa-4,7- diene react with electron-rich arenes in the presence of AlCl3 or H2SO4 to give polyfluorinated phenoxybiaryls.

Perfluoroalkyl sulfur compounds: An unusual reactivity pattern of perfluoroalkanesulfonic esters

Four kinds of perfluoro-or polyfluoroalkanesulfonic esters, namely RFSO3CH2RF, RFSO3CF2RF, RFSO3C6F5 and C6Fsub

Perfluoro- and Polyfluoro-sulphonic Acids. Part 22. Polyfluorophenyl Pentafluorobenzenesulphonates and their Electron Transfer Reaction with Sodium Iodide

Polyfluorophenyl pentafluorobenzenesulphonates (1) have been synthesized in excellent yields by the reaction of pentafluorobenzenesulphonyl chloride with polyfluorophenoxides.Nucleophilic attack on 1 resulted in the breakage of the S-O bond accompanied by displacement of o- and /or p-fluorine.Reaction of 1 with sodium iodide (8) in a mole ratio of 1:3 (1:8) yielded polyfluorodiphenyl ethers 9 and 10 as the main products.However, p-C6F5OC6F4SO3C6F5 (12) was isolated as the major product in addition to 9 and 10 when the reactant ratio was 1:1 or 1:0.25.Reaction of 12 with sodium iodide also gave 9 and 10 when the reactant ratio was 1:3 (12:8).The reaction of 1 (or 12) with NaI is supposed to be an electron-transfer process.