754-43-8

Usage

Uses

Used in Industrial and Commercial Applications:
(2-BROMO)HEXAFLUORO-2-(TRIFLUOROMETHYL)PROPANE is used as a cleaning and degreasing agent for its ability to effectively remove contaminants and grease from surfaces without causing damage or corrosion.
Used in Heat Transfer Applications:
(2-BROMO)HEXAFLUORO-2-(TRIFLUOROMETHYL)PROPANE is used as a heat transfer fluid in various industrial processes due to its high boiling point and thermal stability.
Used as an Environmentally Friendly Solvent:
(2-BROMO)HEXAFLUORO-2-(TRIFLUOROMETHYL)PROPANE is used as a sustainable alternative to traditional solvents in various industries, such as manufacturing, automotive, and electronics, due to its low global warming potential and zero ozone depletion potential.

InChI:InChI=1/C4BrF9/c5-1(2(6,7)8,3(9,10)11)4(12,13)14

Upstream product

• 661-95-0 1,2-dibromohexafluoropropane 
• 382-21-8 perfluoroisobutylene 
• 38568-21-7 2,2-dibromo-1,1,1,3,3,3-hexafluoropropane 
• 85093-71-6 2,3-dibromo-2-trifluoromethyl-3,3-difluoropropionic acid ethyl ester 
• 122432-75-1 1,1,1,2,3,5,5,5-Octafluoro-2,3,4,4-tetrakis-trifluoromethyl-pentane 
• 150746-76-2 tris(dimethylamino)sulfonium trimethylsilyldifluoride 
• 100645-89-4 tris(dimethylamino)sulfonium1,1,1,3,3,3-hexafluoro-2-(trifluoromethyl)-2-propanide 
• 36714-72-4 perfluoro-tert-butylcesium 
• 354-93-8 1,1,1,3,3,3-hexafluoro-2-nitroso-2-trifluoromethyl-propane 

Downstream Products

• 36553-72-7 3,3,3-trifluoro-2,2-bis(trifluoromethyl)propylbenzene 
• 2314-97-8 iodotrifluoromethane 
• 4459-18-1 perfluoro-tert-butyl iodide 
• 382-24-1 1,1,1,3,3,3-hexafluoro-2-trifluoromethyl-propane 

Relevant academic research and scientific papers

Some new chemistry of perfluoro-t-butylsilver

Perfluoro-t-butylsilver, prepared by the reaction of silver fluoride with perfluoroisobutene, has been used to prepare new perfluoro-t-butyl derivatives in good yield.

Pyrolysis of branched-chain perfluoroalkanes in the presence of halogens

The thermal decomposition of some highly branched perfluoroalkanes in the presence of molecular halogens (Cl2, Br2, I2) has been studied.The clear-cut cleavage of the most hindered carbon-carbon bond and the trapping by halogens of the intermediate radicals so formed account for the product distribution.Kinetic measurements support a mechanism based on homolytic rupture of the perfluoroalkanes as the rate-determining step, followed by the fast reaction of the intermediates with halogens.

REACTIONS INVOLVING FLUORIDE ION. PART 34. STABLE PERFLUORINATED CARBANIONS

A remarkable series of perfluoroalkyl anions, generated by reaction of caesium fluoride with various perfluorinated alkenes have been observed by (19)F and (13)C n.m.r. spectroscopy.Trapping experiments are described and threshold temperatures are established for the onset of fluoride ion exchange.The effects of counter ions are compared and (Me2N)3S+ (TAS) salts are more readily produced than Cs+ salts, but exchange of fluoride ion with fluorinated alkenes occurs more readily with TAS salts.Ph4P+ and Bu4N+ salts could not be obtained.Competition experiments for CsF between various perfluoroalkenes has established orders of carbanion stability.

Tris(disubstituted amino)sulfonium perfluorocarbanion salts

Tris(disubstituted amino)sulfonium perfluorocarbanion salts and process for their preparation.

Direct Observation of Simple Fluorinated Carbanions

Simple perfluorinated carbanions are generated and observed by (19)F and (13)C n.m.r. spectroscopy; curious low-field shifts are observed for sites adjacent to the charged centres.