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  2. Bistriflimide - Wikipedia

    en.wikipedia.org/wiki/Bistriflimide

    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. It is a crystalline compound, but is hygroscopic to the point of being deliquescent. Owing to its very high acidity and good compatibility with organic solvents it has been ...

  3. Bis(trifluoromethanesulfonyl)aniline - Wikipedia

    en.wikipedia.org/wiki/Bis(trifluoromethanesulfo...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  4. Lithium bis(trifluoromethanesulfonyl)imide - Wikipedia

    en.wikipedia.org/wiki/Lithium_bis(trifluorome...

    CAS Number. 90076-65-6 ... imide, often simply referred to as LiTFSI, is a hydrophilic salt with the chemical formula LiC 2 F 6 NO 4 S 2. [2]

  5. 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.

  6. Triflidic acid - Wikipedia

    en.wikipedia.org/wiki/Triflidic_acid

    Triflidic acid (IUPAC name: tris[(trifluoromethyl)sulfonyl]methane, abbreviated formula: Tf 3 CH) is an organic superacid.It is one of the strongest known carbon acids and is among the strongest Brønsted acids in general, with an acidity exceeded only by the carborane acids.

  7. Trimethylsilyl trifluoromethanesulfonate - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilyl_trifluorome...

    TMSOTf is quite sensitive toward hydrolysis: (CH 3) 3 SiO 3 SCF 3 + H 2 O → (CH 3) 3 SiOH + HO 3 SCF 3. It is far more electrophilic than trimethylsilyl chloride.. Related to its tendency to hydrolyze, TMSOTf is effective for silylation of alcohols: [2]

  8. Triflyl group - Wikipedia

    en.wikipedia.org/wiki/Triflyl_group

    Triflyl group. In organic chemistry, the triflyl group (systematic name: trifluoromethanesulfonyl group) is a functional group with the formula R−SO 2 CF 3 and structure R−S(=O) 2 −CF 3.

  9. Sodium trifluoromethanesulfinate - Wikipedia

    en.wikipedia.org/wiki/Sodium_trifluoromethanesul...

    Sodium trifluoromethanesulfinate (CF 3 SO 2 Na) is the sodium salt of trifluoromethanesulfinic acid. Together with t-butyl hydroperoxide, an oxidant, this compound was found to be a suitable reagent for introducing trifluoromethyl groups onto electron-rich aromatic compounds by Langlois; this reagent is also known as the Langlois reagent.