1898-91-5

Basic information

• Product Name: decafluorocyclohexanone
• Synonyms: decafluorocyclohexanone;2,2,3,3,4,4,5,5,6,6-decafluorocyclohexanone;2,2,3,3,4,4,5,5,6,6-Decafluorocyclohexan-1-one
• CAS NO: 1898-91-5
• Molecular Formula: C₆F₁₀O
• Molecular Weight: 278.047632
• Mol File: 1898-91-5.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 85.723°C at 760 mmHg
• Flash Point: 22.014°C
• Appearance: /
• Density: 1.732g/cm³
• Vapor Pressure: 68.528mmHg at 25°C
• Refractive Index: 1.29
• CAS DataBase Reference: decafluorocyclohexanone(CAS DataBase Reference)
• NIST Chemistry Reference: decafluorocyclohexanone(1898-91-5)
• EPA Substance Registry System: decafluorocyclohexanone(1898-91-5)

Safety Data

• Hazardous Substances Data: 1898-91-5(Hazardous Substances Data)

Usage

General Description

Decafluorocyclohexanone, also known as perfluorocyclohexanone, is a chemical compound with the molecular formula C6F10O. It is a colorless, odorless liquid that is insoluble in water and has a relatively low boiling point. Decafluorocyclohexanone is used as a solvent and as a reactant in organic synthesis. It is also used in the production of fluoropolymers, and as a precursor to other fluorinated compounds. Due to its high stability and inertness, it has also been studied for potential use as a refrigerant and as a solvent for extracting and separating various compounds. However, it is important to handle decafluorocyclohexanone with caution, as it has been found to be harmful if inhaled or ingested, and may cause irritation to the skin and eyes.

InChI:InChI=1/C6F10O/c7-2(8)1(17)3(9,10)5(13,14)6(15,16)4(2,11)12

Upstream product

• 4943-08-2 methyl undecafluorocyclohexyl ether 
• 5927-67-3 decafluoro-1,2-epoxycyclohexane 
• 4943-06-0 Perfluorcyclohexyl-trifluormethylaether 
• 97843-92-0 1-hydroxy-1-hydroperoxyperfluorocyclohexanone 
• 87901-78-8 perfluoro-1,4-dioxaspiro<4.5>decane 
• 5561-36-4 2,2-Dichlor-perfluor-cyclohexanon 
• 125246-81-3 1-hydroxy-1-(tert-butylperoxy)perfluorocyclohexane 
• 355-75-9 decafluorocyclohex-1-ene 
• 6588-63-2 1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarbonyl fluoride 
• 10363-94-7 1,1,2-Trichlor-2-chlormethoxy-perfluor-cyclohexan 
• 1702-05-2 C₈F₁₃NCl₂ 
• 7732-18-5 water 
• 1702-06-3 (CF₂)5CFNCFF 
• 1702-07-4 (CF₂)5CFNCFCF₃ 

Downstream Products

• 16031-06-4 Perfluorcyclohexyl-2'-jod-1',1'-difluor-aethylaether 
• 125246-81-3 1-hydroxy-1-(tert-butylperoxy)perfluorocyclohexane 
• 5672-50-4 perfluoro-2-cyclohexene-1-one 
• 97843-92-0 1-hydroxy-1-hydroperoxyperfluorocyclohexanone 
• 106813-73-4 α,α'-dihydroxydi(perfluorocyclohexyl)peroxide 
• 74528-69-1 decafluorocyclohexylidenimine 
• 16621-91-3 <1-Hydroxy-perfluor-cyclohexyl>-essigsaeure 
• 16621-88-8 1-Hydro-decafluorcyclohexanol 
• 16621-84-4 decafluorocyclohexan-1,1-diol 
• 16621-89-9 Kalium-perfluor-cyclohexanolat 
• 16621-95-7 perfluorocyclohexyl acrylate 
• 16622-02-9 (Perfluor-cyclohexylidenyl)-essigsaeure-ethylester 
• 217825-01-9 1-pentafluorophenylperfluorocyclohexanol 

Relevant articles and documents

Aerosol Direct Fluorination. Indirect Syntheses of Perfluorocyclic Ketones

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Functionally Substituted Organic Peroxides. XIX. Kinetics of the Reaction of Poly- and Perfluorinated Carbonyl Compounds with tert-Butyl Hydroperoxide

The kinetics of noncatalytic reaction of fluorinated aliphatic and aromatic aldehydes, alkyl, cycloalkyl, and aryl ketones, and β-ketoesters with tert-butyl hydroperoxide were studied by IR spectroscopy.

SYNTHESIS AND SOME CHARACTERISTICS OF 1,2-EPOXYPERFLUOROCYCLOHEXANE

1,2-Epoxyperfluorocyclohexane was obtained with a high yield by the epoxidation of perfluorocyclohexene with an aqueous solution of sodium hypochlorite in the presence of acetonitrile. 1,2-Epoxyperfluorocyclohexane undergoes both nucleophilic and electrop