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  2. Dimethyl sulfoxide - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_sulfoxide

    Dimethyl sulfoxide (DMSO) is an organosulfur compound with the formula (CH 3) 2 S O. This colorless liquid is the sulfoxide most widely used commercially.

  3. Dimethyl sulfoxide (data page) - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_sulfoxide_(data_page)

    Phase behavior Triple point: 291.67 K (18.52 °C), ? Pa Critical point [2]: 720 K (447 °C), 5630 kPa Std enthalpy change of fusion, Δ fus H o: 14.37 kJ/mol Std entropy change

  4. List of water-miscible solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_water-miscible...

    dimethyl sulfoxide: 67-68-5 C 4 H 8 O 2: 1,4-Dioxane: 123-91-1 C 2 H 6 O: ethanol: 64-17-5 CH 3 CH 2 NH 2: ethylamine: 75-04-7 C 2 H 6 O 2: ethylene glycol: 107-21-1 ...

  5. Sulfoxide - Wikipedia

    en.wikipedia.org/wiki/Sulfoxide

    For example, dimethyl sulfide is oxidized to dimethyl sulfoxide and then further to dimethyl sulfone. Unsymmetrical sulfides are prochiral, thus their oxidation gives chiral sulfoxides. This process can be performed enantioselectively. [9] [10] Symmetrical sulfoxides can be formed from a diorganylzinc compound and liquid sulfur dioxide. [11]

  6. 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.

  7. Transition metal sulfoxide complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_sulfoxide...

    The most common sulfoxide ligand is dimethyl sulfoxide (dmso). Many sulfoxides are known because an enormous range of organic substituents are possible. When the two substituents differ, the ligand is chiral. Chiral sulfoxides are configurationally stable. One example is methyl phenyl sulfoxide.

  8. Trimethylsulfoxonium iodide - Wikipedia

    en.wikipedia.org/wiki/Trimethylsulfoxonium_iodide

    It is iodide salt of a common sulfoxonium ions. This compound, a colorless solid, is commercially available. It may be prepared by the alkylation of dimethyl sulfoxide with iodomethane: [1] (CH 3) 2 SO + CH 3 I → (CH 3) 3 SO + I −. The trimethylsulfoxonium ion features a tetrahedral sulfur center. The ion has idealized C 3v symmetry.

  9. Solvent - Wikipedia

    en.wikipedia.org/wiki/Solvent

    Diethylene glycol dimethyl ether: 0.943 N,N-Dimethylformamide 0.944 2-Methoxyethanol 0.965 Pyridine 0.982 Propanoic acid 0.993 Water 1.000 2-Methoxyethyl acetate 1.009 Benzonitrile 1.01 1-Methyl-2-pyrrolidinone 1.028 Hexamethylphosphoramide 1.03 1,4-Dioxane 1.033 Acetic acid 1.049 Acetic anhydride 1.08 Dimethyl sulfoxide 1.092 Chlorobenzene 1.1066

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