79-53-8

Usage

Uses

Used in Chemical Synthesis:
Chloropentafluoroacetone is used as a reagent in the chemical synthesis of various organic compounds. Its ability to modify other compounds by adding CF3 and CF2Cl groups makes it a valuable intermediate in the production of a wide range of chemical products, including pharmaceuticals, agrochemicals, and specialty chemicals.
Used in Polymer Modification:
In the polymer industry, chloropentafluoroacetone is used as a modifying agent to enhance the properties of polymers. The addition of CF3 and CF2Cl groups can improve the thermal stability, chemical resistance, and other performance characteristics of polymers, making them suitable for various applications, such as high-performance plastics, coatings, and adhesives.
Used in Environmental Applications:
Chloropentafluoroacetone can be used in environmental applications, such as the decontamination of hazardous materials and the treatment of industrial waste. Its reactivity allows it to react with and neutralize toxic substances, making it a potential candidate for environmental remediation processes.
Used in Analytical Chemistry:
In analytical chemistry, chloropentafluoroacetone can be employed as a derivatizing agent for the analysis of various organic compounds. The addition of CF3 and CF2Cl groups can improve the detection and quantification of target analytes, enhancing the sensitivity and accuracy of analytical methods.
Used in Specialty Chemicals:
Chloropentafluoroacetone is also used in the production of specialty chemicals, such as surfactants, lubricants, and fire suppressants. The unique properties conferred by the CF3 and CF2Cl groups can provide these products with enhanced performance and stability, making them suitable for specific applications in various industries.

InChI:InChI=1/C3ClF5O/c4-2(5,6)1(10)3(7,8)9

Upstream product

• 116-16-5 1,1,1,3,3,3-hexachloro-propan-2-one 
• 53841-56-8 pentafluoroprop-1-en-2-ol 
• 920-65-0 3,3-dichloro-1,1,1,3-tetrafluoroacetone 
• 51689-98-6 α-(fluorosulfato)pentafluoroacetone 
• 113851-93-7 3-chlorotetrafluoroacetonyl fluorosulfate 
• 684-16-2 Hexafluoroacetone 
• 5068-87-1 3-chloropentafluoropropene-1,2-oxide 

Downstream Products

• 36029-78-4 α-(Chlordifluormethyl)-α,p-bis(trifluormethyl)benzylalkohol 
• 21993-76-0 C₁₅H₁₀BCl₂F₅O 
• 55562-56-6 C₂₄H₂₀ClF₅OSi 
• 36029-76-2 α-(Chlordifluormethyl)-α-(trifluormethyl)-m-fluor-benzylalkohol 
• 36029-79-5 α-(Chlordifluormethyl)-α,m-bis(trifluormethyl)benzylalkohol 
• 13006-19-4 α-(Chlordifluormethyl)-α-(trifluormethyl)-benzylalkohol 
• 36087-08-8 α-(Chlordifluormethyl)-α-(trifluormethyl)-p-methoxy-benzylalkohol 
• 87405-88-7 2-(4-tert-Butyl-phenyl)-1-chloro-1,1,3,3,3-pentafluoro-propan-2-ol 
• 87405-86-5 1-chloro-1,1,3,3,3-pentafluoro-2-<4-(2-methylpropyl)-phenyl>-2-propanol 
• 87405-85-4 1-Chloro-1,1,3,3,3-pentafluoro-2-(4-propyl-phenyl)-propan-2-ol 
• 87405-87-6 1-Chloro-2-(4-cyclohexyl-phenyl)-1,1,3,3,3-pentafluoro-propan-2-ol 
• 87405-84-3 1-chloro-1,1,3,3,3-pentafluoro-2-<4-(2,2-di-methylpropyl)phenyl>-2-propanol 
• 335-42-2 perfluorobutyryl fluoride 
• 431-71-0 1,1,1,3,3-pentafluoro-2-propanone 

Relevant academic research and scientific papers

3-CHLOROPENTAFLUOROPROPENE-1,2-OXIDE: PREPARATION AND REACTIONS WITH SOME HETEROATOM NUCLEOPHILES AND ANTIMONY PENTAFLUORIDE

Nucleophilic epoxidation of 3-chloropentafluoro-1-propene at PTC conditions afforded 3-chloropentafluoropropene-1,2-oxide, which was reacted with some oxygen and nitrogen nucleophiles to 3-chloro-3,3-difluoropropionic acid derivatives.With antimony pentafluoride, mixture of fluorinated acetones was obtained.

Interaction of perfluorinated α-fluorosulfatocarbonyl compounds with nucleophilic reagents

α-Perfluorosulfatoperfluorocarbonyl compounds interact with alkaline metals halogenides to form the corresponding α-halo derivatives as a result of the direct nucleophilic substitution of the FSO3 group.Through the action of halogenide anions on perfluorinated α,β-bis-fluorosulfatocarbonyl compounds, substitution by halogen of the FSO3 group in the α-position to the carbonyl takes place.However, the FSO3 group in the β-position is cleaved, which allows α-substituted β-dicarbonyl derivatives to be obtained.

Preparation of α-halo-F-2-ketones and F-2-ketones via fluorination of α,α-dihalo-F-2-ketones

Fluorination of α,α-dichloro-F-2-ketones with antimony pentafluoride provided excellent yields of α-chloro-F-2-ketones and F-2-ketones regioselectively.However, fluorination of α,α-dibromo-F-2-ketones with antimony pentafluoride gave a mixture of α-bromo-F-2-ketones and F-2-ketones.

FLUOROALIPHATIC ESTERS OF FLUOROSULFONIC ACID. 4. REACTIONS OF α-FLUOROSULFATOPERFLUORO KETONES WITH NUCLEOPHILIC REAGENTS

α-Fluorosulfatoperfluoroethyl isopropyl ketone I and fluorosulfatopentafluoroacetone II react with alkali metal chlorides and bromides to form the corresponding α-haloperfluoro ketones as a result of direct nucleophilic substitution.