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  2. Methylsulfonylmethane - Wikipedia

    en.wikipedia.org/wiki/Methylsulfonylmethane

    Dimethyl sulfone (DMSO 2) is an organosulfur compound with the formula (CH 3) 2 SO 2. It is also known by several other names including methyl sulfone and (especially in alternative medicine) methylsulfonylmethane (MSM). [4] This colorless solid features the sulfonyl functional group and is the simplest of the sulfones. It is relatively inert ...

  3. Dimethyl sulfate - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_sulfate

    Impure dimethyl sulfate was prepared in the early 19th century. [4] J. P. Claesson later extensively studied its preparation. [5] [6]It was investigated for possible use in chemical warfare in World War I [7] [8] in 75% to 25% mixture with methyl chlorosulfonate (CH 3 ClO 3 S) called "C-stoff" in Germany, or with chlorosulfonic acid called "Rationite" in France.

  4. Methyl methanesulfonate - Wikipedia

    en.wikipedia.org/wiki/Methyl_methanesulfonate

    Ethyl methanesulfonate, dimethyl sulfone, dimethyl sulfate Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify ( what is Y N ?)

  5. Dimethyl sulfone - Wikipedia

    en.wikipedia.org/?title=Dimethyl_sulfone&redirect=no

    This page was last edited on 4 November 2007, at 19:45 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  6. Dimethylsulfone reductase - Wikipedia

    en.wikipedia.org/wiki/Dimethylsulfone_reductase

    dimethyl sulfoxide + H 2 O + NAD + dimethyl sulfone + NADH + H + Dimethylsulfone reductase is a molybdoprotein. References External links. Dimethylsulfone+reductase ...

  7. 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.

  8. Deuterated DMSO - Wikipedia

    en.wikipedia.org/wiki/Deuterated_DMSO

    Deuterated DMSO, also known as dimethyl sulfoxide-d 6, is an isotopologue of dimethyl sulfoxide (DMSO, (CH 3) 2 S=O)) with chemical formula ((CD 3) 2 S=O) in which the hydrogen atoms ("H") are replaced with their isotope deuterium ("D"). Deuterated DMSO is a common solvent used in NMR spectroscopy.

  9. Organosulfur chemistry - Wikipedia

    en.wikipedia.org/wiki/Organosulfur_chemistry

    Organosulfur chemistry is the study of the properties and synthesis of organosulfur compounds, which are organic compounds that contain sulfur. [1] They are often associated with foul odors, but many of the sweetest compounds known are organosulfur derivatives, e.g., saccharin.