21652-57-3

Usage

Uses

Used in Chemical Industry:
1-BROMO-1H,1H,2H,2H-PERFLUORODECANE is used as a solvent for its ability to dissolve a wide range of substances and its compatibility with various chemical processes, taking advantage of its stability and resistance to other solvents.
Used in Mechanical Engineering:
In this industry, 1-BROMO-1H,1H,2H,2H-PERFLUORODECANE is used as a lubricant due to its low friction properties, which are beneficial in reducing wear and tear in mechanical components and systems.
Used in Surface Treatment Industry:
1-BROMO-1H,1H,2H,2H-PERFLUORODECANE is utilized as a surface treatment agent, capitalizing on its resistance to environmental factors to provide protective coatings and improve the durability of various materials.
While the specific applications and industries are not explicitly listed in the provided materials, the general uses mentioned have been inferred based on the properties of 1-BROMO-1H,1H,2H,2H-PERFLUORODECANE. It is important to consider the environmental and health implications when using 1-BROMO-1H,1H,2H,2H-PERFLUORODECANE in any application.

InChI:InChI=1/C10H4BrF17/c11-2-1-3(12,13)4(14,15)5(16,17)6(18,19)7(20,21)8(22,23)9(24,25)10(26,27)28/h1-2H2

Upstream product

• 2043-53-0 2-(n-perfluorooctyl)ethyl iodide 
• 678-39-7 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-1-decanol 
• 113823-56-6 toluene-4-sulfonic acid 1,1,2,2-tetrahydroperfluorodecyl ester 

Downstream Products

• 34598-33-9 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecanoic acid 
• 2043-53-0 2-(n-perfluorooctyl)ethyl iodide 
• 133299-39-5 C₁₀H₄F₁₇Cl 
• 361448-55-7 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoro-undecanoic acid 1-phenyl-ethyl ester 
• 344580-05-8 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-Heptadecafluoro-undecanoic acid (R)-1-phenyl-ethyl ester 
• 89373-67-1 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecanoylchloride 
• 6145-09-1 (3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)benzene 
• 165184-83-8 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoro-1-phenylundecan-1-one 

Relevant academic research and scientific papers

Syntheses and properties of fluorous quaternary phosphonium salts that bear four ponytails; new candidates for phase transfer catalysts and ionic liquids

The fluorous tertiary phosphine [Rf6-(CH2) 2]3P [Rfn = CF3(CF2) n-1] and excess PhCH2Br, CH3(CH 2)3OSO2CF3

Ionic transformations in extremely nonpolar fluorous media: Phase transfer catalysis of halide substitution reactions

Fluorous solutions of alkyl halides R18(CH2) mX (m = 2, 3; X = Cl, Br, I) are inert toward solid or aqueous NaCl, NaBr, and Kl, but halide substitution occurs in the presence of fluorous phosphonium salts (10 mol %, 76-100 °C).

Combining lipase-catalyzed enantiomer-selective acylation with fluorous phase labeling: A new method for the resolution of racemic alcohols

Lipase-catalyzed acylation of racemic alcohols with a highly fluorinated acyl donor allows their kinetic resolution accompanied by the simultaneous enantiomer-selective fluorous phase labeling. Both the tagged and the untagged enantiomer can be separated without chromatography by a very efficient partition between a fluorous and an organic phase. The method has been successfully applied to the resolution of typically racemic secondary alcohols of low molecular weight. The fluorous label can be recovered quantitatively.

Separation of enantiomers by extraction based on lipase-catalyzed enantiomer-selective fluorous-phase labeling

No chromatography is necessary to separate a racemic alcohol into its enantiomers. A highly fluorinated acyl residue was tranferred in an enantiomer-selective manner onto a racemic alcohol in the presence of a lipase [Eq. (1)]. The labeled enantiomer was separated from the unlabeled one by a simple but very efficient partition between fluorous and organic phases.