1898-91-5 Usage
Uses
Used in Organic Synthesis:
Decafluorocyclohexanone is utilized as a reactant in organic synthesis, serving as a key component in the formation of various fluorinated compounds. Its unique properties allow it to participate in a range of chemical reactions, contributing to the synthesis of complex organic molecules.
Used in Solvent Applications:
Due to its inertness and stability, decafluorocyclohexanone is employed as a solvent in various chemical processes. It is particularly useful for extracting and separating compounds that are difficult to dissolve in other solvents, making it a valuable asset in the chemical industry.
Used in the Production of Fluoropolymers:
Decafluorocyclohexanone plays a crucial role in the production of fluoropolymers, which are high-performance polymers known for their exceptional chemical resistance, thermal stability, and non-stick properties. Its contribution to the synthesis of these polymers is vital for the development of materials used in a wide array of applications, including coatings, films, and electrical insulation.
Used as a Precursor to Other Fluorinated Compounds:
Given its fluorinated nature, decafluorocyclohexanone is used as a precursor in the synthesis of other fluorinated compounds. These compounds often exhibit unique properties that are beneficial in various industrial and commercial applications, such as pharmaceuticals, agrochemicals, and specialty materials.
Used in Refrigeration:
Decafluorocyclohexanone has been studied for its potential use as a refrigerant due to its chemical stability and low boiling point. Its properties make it a candidate for use in refrigeration systems, where it could offer advantages over traditional refrigerants, such as reduced environmental impact and improved energy efficiency.
Safety Considerations:
It is important to handle decafluorocyclohexanone with caution, as it has been found to be harmful if inhaled or ingested. Additionally, it may cause irritation to the skin and eyes, necessitating proper safety measures during its use and storage.
Check Digit Verification of cas no
The CAS Registry Mumber 1898-91-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,9 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1898-91:
(6*1)+(5*8)+(4*9)+(3*8)+(2*9)+(1*1)=125
125 % 10 = 5
So 1898-91-5 is a valid CAS Registry Number.
InChI:InChI=1/C6F10O/c7-2(8)1(17)3(9,10)5(13,14)6(15,16)4(2,11)12
1898-91-5Relevant academic research and scientific papers
Catalytic synthesis of certain perfluorinated ketones and study of their structure by 19F NMR spectroscopy
Fenichev,Berenblit,Bispen,Lebedev,Moldavskii
, p. 1243 - 1251 (2014/02/14)
An efficient catalyst of a perfluorinated ketone synthesis of a high selectivity in the absence of solvent was proposed. Products of reaction of perfluorinated fluorides of various structures with tetrafluoroethylene and hexafluoropropylene in the presence of efficient catalysts without solvent were examined. The structure of the resulting products and their isomeric composition were identified by 19F NMR spectrscopy. Pleiades Publishing, Ltd., 2013.
Functionally Substituted Organic Peroxides. XIX. Kinetics of the Reaction of Poly- and Perfluorinated Carbonyl Compounds with tert-Butyl Hydroperoxide
Chapurkin
, p. 36 - 40 (2007/10/03)
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
Zapevalov, A. Ya.,Filyakova, T. I.,Peschanskii, N. V.,Kolenko, I. P.,Kodess, M. I.
, p. 1871 - 1874 (2007/10/02)
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
POLYFLUORO-1,2-EPOXY-ALKANES AND -CYCLOALKANES. PART I. PREPARATION OF SOME POLYFLUORO-1,2-EPOXYCYCLOHEXANES
Coe, Paul L.,Mott, Andrew W.,Tatlow, John Colin
, p. 243 - 254 (2007/10/02)
Polyfluorocyclohexenes with hydrogen, bromine, and methoxy substituents yielded the corresponding 1,2-epoxides when treated with aqueous sodium hypochlorite containing some acetonitrile. 4,5-Dibromooctafluoro-1,2-epoxycyclohexane was debrominated with zin
FLUOROCYCLOHEXANES PART XIV 1-H-DECAFLUOROCYCLOHEXYLAMINE
Coe, P. L.,Sleigh, J. H.,Tatlow, J. C.
, p. 339 - 344 (2007/10/02)
1-H-Decafluorocyclohexylamine (V) has been prepared from decafluorocyclohexene (I). (I) gave the corresponding epoxide (II) by reaction with alkaline hydrogen peroxide, reaction of (II) with fluoride ion in sulpholane yielded decafluorocyclohexanone (III)
