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  2. Metaflumizone - Wikipedia

    en.wikipedia.org/wiki/Metaflumizone

    A discontinued variant of ProMeris, called ProMeris Duo or Promeris for Dogs, was indicated for canine use and was a formulated blend of metaflumizone and amitraz. [2] The metaflumizone-only formulation is waterproof and typically remain effective for 30–45 days in a cutaneous application at the base of the neck.

  3. Trifluoromethanol - Wikipedia

    en.wikipedia.org/wiki/Trifluoromethanol

    Colorless liquid Density: 1.5±0.1 g/cm 3: ... trifluoromethanol can be prepared from trifluoromethyl hypochlorite and ... in an aqueous solution displaced by an acid ...

  4. Trifluoromethyl group - Wikipedia

    en.wikipedia.org/wiki/Trifluoromethyl_group

    Trifluoromethyl group covalently bonded to an R group. The trifluoromethyl group is a functional group that has the formula-CF 3. The naming of is group is derived from the methyl group (which has the formula -CH 3), by replacing each hydrogen atom by a fluorine atom. Some common examples are trifluoromethane H– CF 3, 1,1,1-trifluoroethane H ...

  5. Trifluoromethyltrimethylsilane - Wikipedia

    en.wikipedia.org/wiki/Trifluoromethyltrimethylsilane

    Trifluoromethyltrimethylsilane (known as Ruppert-Prakash reagent, TMSCF 3) is an organosilicon compound with the formula CF 3 Si(CH 3) 3.It is a colorless liquid. The compound is a reagent used in organic chemistry for the introduction of the trifluoromethyl group.

  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. Trifluoroacetone - Wikipedia

    en.wikipedia.org/wiki/Trifluoroacetone

    Trifluoracetone is also used in a synthesis of 2-trifluoromethyl-7-azaindoles starting with 2,6-dihalopyridines. The derived chiral imine is used to prepare enantiopure α-trifluoromethyl alanines and diamines by a Strecker reaction followed by either nitrile hydrolysis or reduction.

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