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  2. 10 Vet-Approved Flea Treatments for Your Cat That ... - AOL

    www.aol.com/lifestyle/7-vet-approved-flea...

    Shop safe cat flea treatments and medicines approved by vets, including topical gels, collars, and oral tablets from Revolution, Advantage, Frontline, and more.

  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. Trifluoromethylation - Wikipedia

    en.wikipedia.org/wiki/Trifluoromethylation

    The first to investigate trifluoromethyl groups in relationship to biological activity was F. Lehmann in 1927. [5] An early review appeared in 1958. [6] An early synthetic method was developed by Frédéric Swarts in 1892, [7] based on antimony fluoride. In this reaction benzotrichloride was reacted with SbF 3 to form PhCF 2 Cl and PhCF 3.

  5. 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 ...

  6. Triflic acid - Wikipedia

    en.wikipedia.org/wiki/Triflic_acid

    In the laboratory, triflic acid is useful in protonations because the conjugate base of triflic acid is nonnucleophilic. It is also used as an acidic titrant in nonaqueous acid-base titration because it behaves as a strong acid in many solvents (acetonitrile, acetic acid, etc.) where common mineral acids (such as HCl or H 2 SO 4) are only moderately strong.

  7. Bistriflimide - Wikipedia

    en.wikipedia.org/wiki/Bistriflimide

    Bistriflimidic acid. The conjugate acid of bistriflimide, which is frequently referred to by the trivial name bistriflimidic acid (CAS: 82113-65-3), is a commercially available superacid.

  8. 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.

  9. 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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