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Cyclohexane, undecafluoro(1,1,2,2,3,3,3-heptafluoropropyl)-, also known as perfluoro(1-cyclohexaneethane), is a perfluorinated organic compound with the chemical formula C9F17. It is a colorless, odorless liquid that is highly resistant to chemical reactions due to the strong carbon-fluorine bonds. cyclohexane, undecafluoro(1,1,2,2,3,3,3-heptafluoropropyl)- is a member of the perfluoroalkyl group and is used in various applications, such as in the production of high-performance lubricants, fire-fighting foams, and as a component in the manufacturing of certain plastics and elastomers. Its unique properties, including low surface tension, high thermal stability, and chemical inertness, make it valuable in industrial and commercial settings. However, due to its persistence in the environment and potential health risks, there is ongoing research and regulation regarding its use and disposal.

374-59-4

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374-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 374-59-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 374-59:
(5*3)+(4*7)+(3*4)+(2*5)+(1*9)=74
74 % 10 = 4
So 374-59-4 is a valid CAS Registry Number.

374-59-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,2,3,3,4,4,5,5,6-undecafluoro-6-(1,1,2,2,3,3,3-heptafluoropropyl)cyclohexane

1.2 Other means of identification

Product number -
Other names 1,1,2,2,3,3,4,4,5,5,6-undecafluoro-6-(heptafluoropropyl)cyclohexane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:374-59-4 SDS

374-59-4Downstream Products

374-59-4Relevant academic research and scientific papers

Free radical chemistry. Part 10.1 Addition of acyclic and cyclic alkanes to hexafluoropropene

Chambers, Richard D.,Fuss, Robert W.,Spink, Robert C. H.,Greenhall, Martin P.,Kenwright, Alan M.,Batsanov, Andrei S.,Howard, Judith A. K.

, p. 1623 - 1638 (2007/10/03)

γ-Ray or peroxide initiated reactions of acyclic and cyclic alkanes with hexafluoropropene are described. A variety of perfluorocarbons and polyfluorinated alkenes, di-enes and a tetra-ene were synthesised from these polyfluoroalkylated alkanes. Eliminati

THE SYNTHESIS OF HIGHLY FLUORINATED ALKYLCYCLOHEXANES FOR USE AS OXYGEN CARRIERS AND THE 19F AND 13C NMR SPECTRA OF ALKYLCYCLOHEXANES

Lin, Wen-Huey,Lagow, Richard J.

, p. 345 - 358 (2007/10/02)

Perfluoroalkylcyclohexanes are promising candidates for oxygen carriers.The perfluoroalkylcyclohexane analogues and 1H-perfluoroalkylcyclohexanes of n-propylcyclohexane, i-propylcyclohexane, n-butylcyclohexane, s-butylcyclohexane, i-butylcyclohexane and t-butylcyclohexane were prepared and characterized.Their properties and NMR spectra are discussed.

FREE RADICAL CHEMISTRY, PART 5. A NEW APPROACH TO THE SYNTHESIS OF PERFLUORINATED ETHERS

Chambers, Richard D.,Grievson, Brian,Drakesmith, Frederick G.,Powell, Richard L.

, p. 323 - 340 (2007/10/02)

Fluorinations of the free-radical adducts of fluorinated alkenes, to ethers, over cobalt trifluoride are described and perfluorinated ethers are obtained at temperatures in excess of 400 deg C.The effect of structure on the formation of perfluoroethers is outlined.

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