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  2. Sodium p-toluenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Sodium_p-toluenesulfonate

    Sodium p-toluenesulfonate is an organic compound with the formula CH 3 C 6 H 4 SO 3 Na. It is white, water-soluble solid. It is produced by the neutralization toluenesulfonic acid with sodium hydroxide. It is also a common product from the reactions of sodium-based reagents with toluenesulfonates. [1]

  3. Tosyl group - Wikipedia

    en.wikipedia.org/wiki/Tosyl_group

    The toluenesulfonate (or tosylate) group refers to the −O−SO 2 C 6 H 4 CH 3 (–OTs) group, with an additional oxygen attached to sulfur and open valence on an oxygen. [3] In a chemical name, the term tosylate may either refer to the salts containing the anion of p -toluenesulfonic acid, TsO − M + (e.g., sodium p-toluenesulfonate ), or it ...

  4. p-Toluenesulfonic acid - Wikipedia

    en.wikipedia.org/wiki/P-Toluenesulfonic_acid

    p-Toluenesulfonic acid (PTSA, pTSA, or pTsOH) or tosylic acid (TsOH) is an organic compound with the formula CH 3 C 6 H 4 SO 3 H. It is a white extremely hygroscopic solid that is soluble in water, alcohols, and other polar organic solvents. [6] The CH 3 C 6 H 4 SO 2 group is known as the tosyl group and is often abbreviated as Ts or Tos.

  5. Diazald - Wikipedia

    en.wikipedia.org/wiki/Diazald

    Diazald (N-methyl-N-nitroso-p-toluenesulfonamide) is used as a relatively safe and easily handled precursor to diazomethane, which is toxic and unstable. [2] Diazald has become the favored commercially available precursor for the synthesis of diazomethane, compared to reagents like N-methyl-N-nitrosourea and N-methyl-N'-nitro-N-nitrosoguanidine, which are less thermally stable and more toxic ...

  6. Desulfonylation reactions - Wikipedia

    en.wikipedia.org/wiki/Desulfonylation_reactions

    Desulfonylation reactions are chemical reactions leading to the removal of a sulfonyl group from organic compounds. As the sulfonyl functional group is electron -withdrawing, [ 1 ] methods for cleaving the sulfur –carbon bonds of sulfones are typically reductive in nature.

  7. TPPTS - Wikipedia

    en.wikipedia.org/wiki/Tppts

    3,3′,3′′-Phosphanetriyltris(benzenesulfonic acid) trisodium salt (abbreviated TPPTS), is an organic compound that is also known as sodium triphenylphosphine trisulfonate. The compound has the formula P(C 6 H 4 SO 3 Na) 3. This white solid is an unusual example of a water-soluble phosphine. Its complexes are also water-soluble. [2]

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  9. 4-Toluenesulfonyl chloride - Wikipedia

    en.wikipedia.org/wiki/4-Toluenesulfonyl_chloride

    4-Toluenesulfonyl chloride (p-toluenesulfonyl chloride, toluene-p-sulfonyl chloride) is an organic compound with the formula CH 3 C 6 H 4 SO 2 Cl. This white, malodorous solid is a reagent widely used in organic synthesis. [2] Abbreviated TsCl or TosCl, it is a derivative of toluene and contains a sulfonyl chloride (−SO 2 Cl) functional group.

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