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Bis(perfluoro-n-propyl)disulfane, also known as 1,1'-Disulfanediyldiperfluoropropane, is a chemical compound with the molecular formula C6H2F12S2. It is a colorless liquid at room temperature and is characterized by its strong, pungent odor. bis(perfluoro-n-propyl)disulfane is composed of two perfluoro-n-propyl groups connected by a disulfide bridge. Bis(perfluoro-n-propyl)disulfane is primarily used as a precursor in the synthesis of various perfluoropolyethers, which are utilized in a range of applications, including lubricants, surfactants, and materials for extreme environments. Due to its reactivity and potential hazards, it is essential to handle this chemical with proper safety measures and in accordance with established guidelines.

356-07-0

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356-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 356-07-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 356-07:
(5*3)+(4*5)+(3*6)+(2*0)+(1*7)=60
60 % 10 = 0
So 356-07-0 is a valid CAS Registry Number.

356-07-0Relevant academic research and scientific papers

Free-Radical Reactions of Fluoroalkanesulfenyl Halides. 4. Reactions of Perfluoroalkane- and Pentafluorobenzenesulfenyl Chlorides with Hydrocarbons in the Presence of Fluorinated Disulfides

Harris, J. F.

, p. 268 - 271 (2007/10/02)

Free-radical reactions of perfluoroalkanesulfenyl chlorides and pentafluorobenzenesulfenyl chloride with cyclohexane and toluene were carried out in the presence of bis(perfluoroalkyl) disulfides and bis(pentaflurophenyl)disulfide to assess the competition between the disulfide and the sulfenyl chloride for reaction with hydrocarbon radicals.With added bis(perfluoroalkyl) disulfides, radical attack occurs only on the sulfenyl chloride, but with added bis(pentafluorophenyl) disulfide, attack occurs on both sulfenyl chloride and disulfide.

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