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  2. Fluoroalcohol - Wikipedia

    en.wikipedia.org/wiki/Fluoroalcohol

    Fluoroalcohol. 3 languages. 日本語 ... Printable version; In other projects ... [1] Perfluoroalcohols. Most primary and secondary perfluoroalcohols are unstable, ...

  3. Fluorotelomer alcohol - Wikipedia

    en.wikipedia.org/wiki/Fluorotelomer_alcohol

    [5] [6] FTOHs can also be used as intermediates in the production of surfactants. [7] Fluorotelomer alcohols can biodegrade to perfluorinated carboxylic acids, which persist in the environment and are found in the blood serum of populations and wildlife, such as the toxic PFOA and PFNA. [8] [9] Aerobic biotransformation pathways of 8:2 FTOH in ...

  4. Pentafluorophenol - Wikipedia

    en.wikipedia.org/wiki/Pentafluorophenol

    Pentafluorophenol is the organofluorine compound (specifically a fluoroalcohol) with the formula C 6 F 5 OH. This is the perfluorinated analogue of phenol. It is a white solid that melts just above room temperature, and smells of phenol. With a pK a of 5.5, it is one of the most acidic phenols.

  5. 2-Fluoroethanol - Wikipedia

    en.wikipedia.org/wiki/2-Fluoroethanol

    2-Fluoroethanol was originally synthesized by treating 2-chloroethanol with potassium fluoride, in a simple Finkelstein reaction. [5] The product has a lower boiling point that the starting material and may be conveniently isolated by distillation.

  6. Perfluorinated compound - Wikipedia

    en.wikipedia.org/wiki/Perfluorinated_compound

    They are components of fire-fighting foam. [1] Fluorosurfactants (PFAS) reduce surface tension by concentrating at the liquid-air interface due to the lipo phobicity of polyfluorocarbons. Chlorofluorocarbons are also perfluorinated compounds, many of which were formerly used as refrigerants ( Freon ) until they were implicated in ozone ...

  7. Hexafluoro-2-propanol - Wikipedia

    en.wikipedia.org/wiki/Hexafluoro-2-propanol

    Hexafluoro-propan-2-ol is a speciality solvent for organic synthesis, particularly for reactions involving oxidations and strong electrophiles. For example, HFIP enhances the reactivity of hydrogen peroxide as applied to Baeyer-Villiger oxidation of cyclic ketones. [ 1 ]

  8. Nonafluoro-tert-butyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Nonafluoro-tert-butyl_alcohol

    Nonafluoro-tert-butyl alcohol (IUPAC name: 1,1,1,3,3,3-hexafluoro-2-(trifluoromethyl)propan-2-ol) is a fluoroalcohol. It is the perfluorinated analog of tert -butyl alcohol . Notably, as a consequence of its electron withdrawing fluorine substituents, it is very acidic for an alcohol, with a p K a value of 5.4, similar to that of a carboxylic acid.

  9. Template:Metabolic pathways - Wikipedia

    en.wikipedia.org/wiki/Template:Metabolic_pathways

    This page is the template for the metabolic pathways template. This template should be used to illustrate the general 'shape' of metabolism within the cell. This template is part of the Metabolic Pathways task force. This template has been largely superseded by {{Metabolic metro}} but is kept as an archive