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Usage

Uses

Used in Chemical Industry:
1H,1H,1H,3H,3H-PERFLUORONONAN-2-ONE is used as a solvent for various chemical processes, leveraging its high thermal and chemical stability to facilitate reactions in a controlled and efficient manner.
Used in Manufacturing of Perfluorinated Compounds:
As a precursor, 1H,1H,1H,3H,3H-PERFLUORONONAN-2-ONE is instrumental in the production of other perfluorinated compounds, contributing to the development of materials with unique properties for specialized applications.
Used in Specialty Polymers Production:
1H,1H,1H,3H,3H-PERFLUORONONAN-2-ONE is utilized as a key ingredient in the synthesis of specialty polymers, enhancing their performance characteristics for use in demanding environments.
Used in Surfactant Formulation:
This perfluorinated ketone is employed in the formulation of surfactants, improving their effectiveness in various applications such as in the production of foams, emulsions, and wetting agents.
Used in Coating Industry:
1H,1H,1H,3H,3H-PERFLUORONONAN-2-ONE is used as a component in the development of high-performance coatings, capitalizing on its stability to produce durable and long-lasting finishes.

InChI:InChI=1/C9H5F13O/c1-3(23)2-4(10,11)5(12,13)6(14,15)7(16,17)8(18,19)9(20,21)22/h2H2,1H3

Upstream product

• 108-22-5 Isopropenyl acetate 
• 375-85-9 perfluoroheptanoic acid 
• 116-11-0 2-Methoxypropene 
• 355-43-1 n-perfluorohexyl iodide 
• 1833-53-0 2-(Trimethylsilyloxy)propene 
• 38565-52-5 2-(2,2,3,3,4,4,5,5,6,6,7,7,7-tridecafluoroheptyl)oxirane 
• 80363-03-7 3-(F-hexyl)propan-2-ol 

Downstream Products

• 75824-01-0 methyl-1 F-pentyl-3 propanedione-1,3 

Relevant academic research and scientific papers

One-pot reaction for the synthesis of fluorinated β-diketones

Fluorinated β-diketones have been synthesized in high yield from the one-pot reaction of silyl enol ethers with perfluoroalkyl iodides initiates with Na2S2O4/NaHCO3, followed by treatment with diethylamine and acid hydrolysis.

ELECTROCHEMICAL SYNTHESIS OF PERFLUOROALKYLACETONES

The interaction of electrochemically generated radicals in the electrolysis of the perfluorocarboxylic acids RFCF2COOH (I), where RF = F (a), CF3 (b), C2F5 (c), C3F7 (d), C5F11 (e). and C7F15 (f), with isoprenyl acetate (II) was studied.The dependence of the results of the electrolysis on the adsorption capacity of the anode permits the proposition that the interaction of (II) with the ECG-radicals occurs close to the surface of the electrode.The yield of the perfluoroalkylacetones comprised 30-37percent.

Annelation d'enamines par les cetones α,β-ethyleniques fluorees. VI (1): Reaction d'aromatisation

Various perfluoroalkylacetones were prepared by addition of perfluoroalkyliodides to 2-methoxypropene and condensed with 1-pyrrolidinocyclopentene or -cyclohexene.An annelation-aromatisation process led to 4-perfluoroalkyl-6-pyrrolidinoindanes and 1-perfluoroalkyl-3-pyrrolidino-5,6,7,8-tetrahydronaphthalenes.

A Carbon-13 Nuclear Magnetic Resonance Study of Compounds Substituted by a Perfluoroalkyl Chain

The 13C NMR spectra of alkanes, alkanones and cyclohexanones substituted by perfluoroalkyl groups, RF, have been studied.The influence of the perfluoroalkyl group on the chemical shifts of other carbons of the molecules is the same regardless of the RF chain length.