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  2. Methanesulfonic acid - Wikipedia

    en.wikipedia.org/wiki/Methanesulfonic_acid

    Methanesulfonic acid (MsOH, MSA) or methanesulphonic acid (in British English) is an organosulfuric, colorless liquid with the molecular formula CH 3 SO 3 H and structure H 3 C−S(=O) 2 −OH. It is the simplest of the alkylsulfonic acids ( R−S(=O) 2 −OH ).

  3. Sulfonic acid - Wikipedia

    en.wikipedia.org/wiki/Sulfonic_acid

    Sulfonic acids are strong acids. They are commonly cited as being around a million times stronger than the corresponding carboxylic acid. For example, p-Toluenesulfonic acid and methanesulfonic acid have pK a values of −2.8 and −1.9, respectively, while those of benzoic acid and acetic acid are 4.20 and 4.76, respectively

  4. Methanesulfonyl azide - Wikipedia

    en.wikipedia.org/wiki/Methanesulfonyl_azide

    Methanesulfonyl azide melts at 18 °C and decomposes from 120 °C. [1] Like many other azides, it is explosive. [3] At low temperature, methanesulfonyl azide crystallizes in the triclinic crystal system in the space group P1 with the lattice parameters a = 5.6240 Å; b = 5.9498 Å, c = 7.6329 Å, α = 72.216°, β = 70.897°, and γ = 88.601°, and two molecules per unit cell.

  5. Methanesulfonyl chloride - Wikipedia

    en.wikipedia.org/wiki/Methanesulfonyl_chloride

    Methanesulfonyl chloride is mainly used to give methanesulfonates by its reaction with alcohols in the presence of a non-nucleophilic base. [8] In contrast to the formation of toluenesulfonates from alcohols and p-toluenesulfonyl chloride in the presence of pyridine, the formation of methanesulfonates is believed to proceed via a mechanism wherein methanesulfonyl chloride first undergoes an ...

  6. Methanesulfonic anhydride - Wikipedia

    en.wikipedia.org/wiki/Methanesulfonic_anhydride

    Methanesulfonic anhydride (Ms 2 O) is the acid anhydride of methanesulfonic acid. Like methanesulfonyl chloride (MsCl), it may be used to generate mesylates (methanesulfonyl esters). Preparation & purification

  7. Ethyl methanesulfonate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_methanesulfonate

    Ethyl methanesulfonate (EMS) is an organosulfur compound with the formula CH 3 SO 3 C 2 H 5.It is the ethyl ester of methanesulfonic acid.A colorless liquid, it is classified as an alkylating agent.

  8. Methyl methanesulfonate - Wikipedia

    en.wikipedia.org/wiki/Methyl_methanesulfonate

    Methanesulfonic acid methyl ester Methyl mesylate MMS. Identifiers CAS Number. 66-27-3 ...

  9. 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.