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  2. Trifluorotoluene - Wikipedia

    en.wikipedia.org/wiki/Trifluorotoluene

    A derivative of trifluorotoluene, 3-aminobenzotrifluoride, is the precursor to the herbicide fluometuron. [3] It is synthesized via nitration followed by reduction to meta-H 2 NC 6 H 4 CF 3. This aniline is then converted to the urea. Flumetramide (6-[4-(trifluoromethyl)phenyl]morpholin-3-one), a skeletal muscle relaxant, is also prepared from ...

  3. Benzonitrile - Wikipedia

    en.wikipedia.org/wiki/Benzonitrile

    Benzonitrile is the chemical compound with the formula C 6 H 5 (CN), abbreviated PhCN. This aromatic organic compound is a colorless liquid with a sweet bitter almond odour. It is mainly used as a precursor to the resin benzoguanamine .

  4. Thiazyl fluoride - Wikipedia

    en.wikipedia.org/wiki/Thiazyl_fluoride

    Thiazyl fluoride, NSF, is a colourless, pungent gas at room temperature and condenses to a pale yellow liquid at 0.4 °C. [1] Along with thiazyl trifluoride, NSF 3, it is an important precursor to sulfur-nitrogen-fluorine compounds. It is notable for its extreme hygroscopicity.

  5. Trifluoroacetic acid - Wikipedia

    en.wikipedia.org/wiki/Trifluoroacetic_acid

    TFA is the precursor to many other fluorinated compounds such as trifluoroacetic anhydride, trifluoroperacetic acid, and 2,2,2-trifluoroethanol. [4] It is a reagent used in organic synthesis because of a combination of convenient properties: volatility, solubility in organic solvents , and its strength as an acid. [ 7 ]

  6. 4-Cyano-3-(trifluoromethyl)aniline - Wikipedia

    en.wikipedia.org/wiki/4-Cyano-3-(trifluoromethyl...

    4-Cyano-3-(trifluoromethyl)aniline, also known as 4-amino-2-(trifluoromethyl)benzonitrile, is a cyanated and trifluoromethylated derivative of aniline. It is the starting material in one of the chemical syntheses of the nonsteroidal antiandrogen bicalutamide .

  7. Trifluoroacetonitrile - Wikipedia

    en.wikipedia.org/wiki/Trifluoroacetonitrile

    [2] [3] This synthesis route was first described by Frédéric Swarts in 1922. [4] Trifluoroacetonitrile can also be produced by reacting 1,1,1-trichloro-2,2,2-trifluoroethane and ammonia at 610 °C. [5]

  8. 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 ...

  9. Trifluoroiodomethane - Wikipedia

    en.wikipedia.org/wiki/Trifluoroiodomethane

    Trifluoroiodomethane contains carbon, fluorine, and iodine atoms. Although iodine is several hundred times more efficient at destroying stratospheric ozone than chlorine, experiments have shown that because the weak C-I bond breaks easily under the influence of water (owing to the electron-attracting fluorine atoms), trifluoroiodomethane has an ozone depleting potential less than one ...