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  2. Fluoroalcohol - Wikipedia

    en.wikipedia.org/wiki/Fluoroalcohol

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us

  3. 2-Fluoroethanol - Wikipedia

    en.wikipedia.org/wiki/2-Fluoroethanol

    2-[18 F]-fluoroethoxy group is a common moiety in the structures of radiotracers used with PET. Such radiotracers include fluoroethyl-l-tyrosine 1-(2-[ 18 F]-fluoroethoxy)-4-nitrobenzene and [ 18 F]-fluoroethyl 4-fluorobenzoate, being a [18F]fluoroalkyl ether and ester respectively.

  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. Pharmacology of ethanol - Wikipedia

    en.wikipedia.org/wiki/Pharmacology_of_ethanol

    All organisms produce alcohol in small amounts by several pathways, primarily through fatty acid synthesis, [70] glycerolipid metabolism, [71] and bile acid biosynthesis pathways. [72] Fermentation is a biochemical process during which yeast and certain bacteria convert sugars to ethanol, carbon dioxide, as well as other metabolic byproducts.

  6. 2,2,2-Trifluoroethanol - Wikipedia

    en.wikipedia.org/wiki/2,2,2-Trifluoroethanol

    Trifluoroethanol is produced industrially by hydrogenation or the hydride reduction of derivatives of trifluoroacetic acid, such as the esters or acyl chloride. [1]TFE can also be prepared by hydrogenolysis of compounds of generic formula CF 3 −CHOH−OR (where R is hydrogen or an alkyl group containing from one to eight carbon atoms), in the presence of a palladium containing catalyst ...

  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. Purine nucleotide cycle - Wikipedia

    en.wikipedia.org/wiki/Purine_nucleotide_cycle

    The Purine Nucleotide Cycle is a metabolic pathway in protein metabolism requiring the amino acids aspartate and glutamate. The cycle is used to regulate the levels of adenine nucleotides, in which ammonia and fumarate are generated. [2] AMP converts into IMP and the byproduct ammonia.

  9. Organofluorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organofluorine_chemistry

    Other biologically synthesized organofluorines include ω-fluoro fatty acids, fluoroacetone, and 2-fluorocitrate which are all believed to be biosynthesized in biochemical pathways from the intermediate fluoroacetaldehyde. [26] Adenosyl-fluoride synthase is an enzyme capable of biologically synthesizing the carbon–fluorine bond. [28]