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  2. File:Dimethyl-disulfide-from-xtal-Mercury-3D-sf.png - Wikipedia

    en.wikipedia.org/wiki/File:Dimethyl-disulfide...

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  3. Dimethyl sulfide - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_sulfide

    Dimethyl sulfide (DMS) or methylthiomethane is an organosulfur compound with the formula (CH 3) 2 S. It is the simplest thioether and has a characteristic disagreeable odor. It is a flammable liquid that boils at 37 °C (99 °F).

  4. File:Dimethyl-disulfide-from-xtal-Mercury-3D-bs.png - Wikipedia

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  5. File:Dimethyl sulfide structure.svg - Wikipedia

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  6. Lignosulfonates - Wikipedia

    en.wikipedia.org/wiki/Lignosulfonates

    The primary site for ether cleavage is the α-carbon (carbon atom attached to the aromatic ring) of the propyl (linear three carbon) side chain. The following structures do not specify the structure since lignin and its derivatives are complex mixtures: the purpose is to give a general idea of the structure of lignosulfonates.

  7. Borane dimethylsulfide - Wikipedia

    en.wikipedia.org/wiki/Borane_dimethylsulfide

    It is an adduct between borane molecule (BH 3) and dimethyl sulfide molecule (S(CH 3) 2). It is a complexed borane reagent that is used for hydroborations and reductions . The advantages of BMS over other borane reagents, such as borane-tetrahydrofuran , are its increased stability and higher solubility. [ 1 ]

  8. Dimethyl sulphide - Wikipedia

    en.wikipedia.org/?title=Dimethyl_sulphide&...

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  9. Dimethylsulfide - Wikipedia

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

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