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Cyclohexane, undecafluoro(trifluoromethoxy)-, also known as perfluorinated cyclohexane trifluoromethyl ether, is a synthetic chemical compound with the molecular formula C7F13O. It is a colorless, odorless, and non-toxic liquid that is highly resistant to thermal and chemical degradation. Cyclohexane, undecafluoro(trifluoromethoxy)- is characterized by its unique structure, where a cyclohexane ring is substituted with eleven fluorine atoms and a trifluoromethoxy group. Due to its exceptional chemical stability, low surface tension, and high dielectric constant, it has potential applications in various industries, such as electronics, aerospace, and pharmaceuticals, particularly as a solvent, lubricant, or insulating fluid. However, its environmental persistence and potential health risks require careful handling and regulation.

4943-06-0

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4943-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4943-06-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,4 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4943-06:
(6*4)+(5*9)+(4*4)+(3*3)+(2*0)+(1*6)=100
100 % 10 = 0
So 4943-06-0 is a valid CAS Registry Number.

4943-06-0Downstream Products

4943-06-0Relevant articles and documents

Prevention of anode fouling during the electrochemical perfluorination of aromatic carboxylic acid chlorides

Ilayaraja,Velayutham,Noel

experimental part, p. 656 - 661 (2009/12/22)

The electrochemical perfluorination of benzoyl chloride, p-substituted benzoyl chlorides and cyclo-hexane carboxylic acid chloride in anhydrous hydrogen fluoride (AHF) medium on nickel electrode is reported. Experimental conditions suppressing polymeric f

ON THE ELECTOCHEMICAL FLUORINATION OF AMINOETHERS TO GIVE PERFLUOROAMINOETHERS: POSSIBLE CANDIDATES FOR BLOOD SUBSTITUTES

Dimitrov, A.,Radeck, W.,Ruediger, St.,Platonov, V.E.

, p. 317 - 331 (2007/10/02)

Aminoethers, (R=C6H5, C6F5, C2H5), C6F5OC2H4N(CH2)5, were electrofluorinated in anhydrous hydrogen fluoride, the corresponding saturated perfluoroaminoethers being the largest individual substances in each case.One of them, F-4-(2-cyclohexyloxy

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