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Cyclopentanemethanol, 1,2,2,3,3,4,4,5-octafluoro- is a fluorinated organic compound with the chemical formula C5HF8O. It features a cyclopentane ring with a hydroxyl group (-OH) attached to one of the carbon atoms and eight fluorine atoms substituting the hydrogen atoms on the ring. Cyclopentanemethanol, 1,2,2,3,3,4,4,5-octafluoro- is characterized by its unique structure, which provides it with distinct chemical and physical properties. Due to its fluorinated nature, it exhibits enhanced stability, reactivity, and solubility compared to its non-fluorinated counterparts. Cyclopentanemethanol, 1,2,2,3,3,4,4,5-octafluoro- has potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science, where its unique properties can be exploited for specific purposes.

7481-14-3

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7481-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7481-14-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,8 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7481-14:
(6*7)+(5*4)+(4*8)+(3*1)+(2*1)+(1*4)=103
103 % 10 = 3
So 7481-14-3 is a valid CAS Registry Number.

7481-14-3Downstream Products

7481-14-3Relevant academic research and scientific papers

Free Radical Chemistry. Part 3. Substituent Effects in Additions of Ethers to Fluorinated Alkenes

Chambers, Richard D.,Grievson, Brian,Kelly, Noel M.

, p. 2209 - 2214 (2007/10/02)

Systematic studies on free-radical addition of acyclic ethers to hexafluoropropene reveal the influence of steric effects on the competitive formation of mono-, di-, and tri-adducts.It is concluded that 'captodative' effects are not dominant in systems containing polyfluoroalkyl groups.Remarkably efficient free-radical additions of trialkyl borates, to fluorinated alkenes occur, but in a series X-OMe (X=MeCO, HCO, MeOCO etc.) reactivity is reduced by electron withdrawal.

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