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  2. Sodium methylsulfinylmethylide - Wikipedia

    en.wikipedia.org/wiki/Sodium_methylsulfinylmethylide

    Sodium methylsulfinylmethylide (also called NaDMSO or dimsyl sodium) is the sodium salt of the conjugate base of dimethyl sulfoxide. This unusual salt has some uses in organic chemistry as a base and nucleophile. Since the first publication in 1965 by Corey et al., [2] a number of additional uses for this reagent have been identified. [3]

  3. 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 ...

  4. Solubility chart - Wikipedia

    en.wikipedia.org/wiki/Solubility_chart

    The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.

  5. Methanesulfonic acid - Wikipedia

    en.wikipedia.org/wiki/Methanesulfonic_acid

    It is based on a direct reaction between methane and oleum at around 50 °C and 100 bar in the presence of a potassium persulfate initiator. [10] Further addition of sulfur trioxide gives methanedisulfonic acid instead. [11] This technology was acquired and commercialized by BASF in 2019. [12]

  6. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    In organic chemistry, a methyl group is an alkyl derived from methane, containing one carbon atom bonded to three hydrogen atoms, having chemical formula CH 3 (whereas normal methane has the formula CH 4). In formulas, the group is often abbreviated as Me. This hydrocarbon group occurs in many organic compounds. It is a very stable group in ...

  7. List of inorganic compounds - Wikipedia

    en.wikipedia.org/wiki/List_of_inorganic_compounds

    Potassium sodium tartrate – KNaC 4 H 4 O 6; Potassium sulfate – K 2 SO 4; Potassium sulfite – K 2 SO 3; Potassium sulfide – K 2 S; Potassium tartrate – K 2 C 4 H 4 O 6; Potassium tetraiodomercurate(II) – K 2 HgI 4; Potassium thiocyanate – KSCN; Potassium titanyl phosphate – KTiOPO 4; Potassium vanadate – KVO 3; Tripotassium ...

  8. Trimethylsulfoxonium - Wikipedia

    en.wikipedia.org/wiki/Trimethylsulfoxonium

    Treated with sodium hydride, trimethylsulfoxonium forms dimethylsulfoxonium methylide. [1] Trimethylsulfoxonium can polymerise to yield polyethylene. [2] [3] Copper, zinc and palladium ions in water react with trimethylsulfoxonium and sodium hydroxide to form sulfur ylide complexes. [4]

  9. Sulfur compounds - Wikipedia

    en.wikipedia.org/wiki/Sulfur_compounds

    Reduction of sulfur gives various polysulfides with the formula S x 2-, many of which have been obtained crystalline form. Illustrative is the production of sodium tetrasulfide: 4 Na + S 8 → 2 Na 2 S 4. Some of these dianions dissociate to give radical anions, such as S 3 − gives the blue color of the rock lapis lazuli.

  1. Related searches methane sulphinylmethane dimethyl sulfur sodium phosphate potassium hydroxide

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    methanesulfonic acid salts