4100-99-6

Usage

Uses

Used in Scientific Research:
1,2-BIS(4'-FLUOROPHENYL)-1,1,2,2-TETRAFLUOROETHANE is used as a research chemical for [application reason], given its unique structure and properties. The presence of fluorine atoms may offer specific benefits in certain research contexts, such as enhancing the stability of the compound or affecting its reactivity. Due to its limited commercial availability, it is primarily utilized in specialized studies where its characteristics are of particular interest.

Upstream product

• 579-39-5 1,2-bis(4-fluorophenyl)ethane-1,2-dione 
• 402-42-6 4-fluoro-1-trichloromethylbenzene 
• 565-04-8 α,α,α',α'-tetrachloro-4,4'-difluoro-bibenzyl 

Downstream Products

• 4246-82-6 1,1,2,2-Tetrafluor-1,2-bis-<4-fluor-3-nitro-phenyl>-aethan 
• 4102-39-0 1,1,2,2-Tetrafluor-1,2-bis-<3-amino-4-fluor-phenyl>-aethan 
• 107233-47-6 1,2-bis[4-(2-hydroxyethoxy)phenyl]-1,1,2,2-tetrafluoroethane 
• 477529-31-0 1,2-di(4-benzyloxyphenyl)tetrafluoroethane 

Relevant academic research and scientific papers

Silver-catalyzed decarboxylative homocoupling reaction for the construction of tetrafluoroethylene-bridging aromatic compounds

The Ag(I)-catalyzed decarboxylative homocoupling from the difluoroacetate has been developed to the synthesis of symmetric CF2–CF2 containing dimers. This radical dimerization overpasses the prefunctionalization of the substrate and provides a direct and efficient method for construction of tetrafluoroethylene bridge-linked homodimers.

Direct nucleophilic fluorination of carbonyl groups of benzophenones and benzils with Deoxofluor

The carbonyl groups of diaryl ketones and diaryl diketones were directly fluorinated with bis(2-methoxyethyl)aminosulfur trifluoride (Deoxofluor) under neat conditions to give the corresponding gem-difluorides and tetrafluorinated derivatives in moderate

Reductive dimerization of dithianylium salts and fluorodesulfuration: A new synthetic approach to tetrafluoroethylene substructures

The reductive dimerization of dithianylium ions, followed by oxidative fluorodesulfuration, opens a convenient access to a variety of 1,2-disubstituted tetrafluoroethylene derivatives. A similar method leads to hexafluorodiacetyl, a potential building blo

Fluorine-containing bisphenols, their preparation, their precursors and intermediates, and use of the fluorine-containing bisphenols

This invention relates to 1,2-di(4-hydroxyaryl)tetrafluoroethanes of the general formula (I) wherein R are each, independently of one another, hydrogen, F, Cl, Br, I, CN, COOR2, C1-C4-alkyl, C1-C4-alk