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  2. Bis(trifluoromethanesulfonyl)aniline - Wikipedia

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

    Bis(trifluoromethanesulfonyl)aniline is the organic compound with the formula C 6 H 5 N(SO 2 CF 3) 2. [1] It is a white solid. The compound is used to install the triflyl group (SO 2 CF 3). Its behavior is akin to that of triflic anhydride, but milder.

  3. 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.

  4. Bistriflimide - Wikipedia

    en.wikipedia.org/wiki/Bistriflimide

    [1] Its p K a value in water cannot be accurately determined but in acetonitrile it has been estimated as −0.10 and in 1,2-dichloroethane −12.3 (relative to the p K a value of 2,4,6-trinitrophenol ( picric acid ), anchored to zero to crudely approximate the aqueous p K a scale [ 2 ] ), making it more acidic than triflic acid (p K a MeCN = 0 ...

  5. Trifluoromethylation - Wikipedia

    en.wikipedia.org/wiki/Trifluoromethylation

    An early report (1949) describes the photochemical reaction of iodotrifluoromethane with ethylene to 3-iodo-1,1,1-trifluoropropane. [53] Reagents that have been reported for the direct trifluoromethylation of arenes are CF 3 I, CF 3 Br (thermal or photochemical), silver trifluoroacetate /TiO 2 (photochemical) and sodium ...

  6. Lithium bis(trifluoromethanesulfonyl)imide - Wikipedia

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

    This page was last edited on 25 January 2025, at 20:59 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  7. PMSF - Wikipedia

    en.wikipedia.org/wiki/PMSF

    The half-life is short in aqueous solutions (110 min at pH 7, 55 min at pH 7.5, and 35 min at pH 8, all at 25 °C). [2] At 4˚C, pH 8, PMSF is almost completely degraded after 1 day. [ 2 ] Stock solutions are usually made up in anhydrous ethanol , isopropanol , or corn oil and diluted immediately before use.

  8. Triflic acid - Wikipedia

    en.wikipedia.org/wiki/Triflic_acid

    With a K a = 5 × 10 14, pK a = −14.7 ± 2.0, [1] triflic acid qualifies as a superacid. It owes many of its useful properties to its great thermal and chemical stability. Both the acid and its conjugate base CF 3 SO − 3, known as triflate, resist oxidation/reduction reactions, whereas many strong acids are oxidizing, such as perchloric or ...

  9. 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.