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  2. Dichloromethane - Wikipedia

    en.wikipedia.org/wiki/Dichloromethane

    DCM is produced by treating either chloromethane or methane with chlorine gas at 400–500 °C. At these temperatures, both methane and chloromethane undergo a series of reactions producing progressively more chlorinated products.

  3. Methyldichloroarsine - Wikipedia

    en.wikipedia.org/wiki/Methyldichloroarsine

    Methyldichloroarsine, sometimes abbreviated "MD" and also known as methyl Dick, [1] is an organoarsenic compound with the formula CH 3 AsCl 2. This colourless volatile liquid is a highly toxic vesicant that has been used in chemical warfare .

  4. Tetramethylammonium chloride - Wikipedia

    en.wikipedia.org/wiki/Tetramethylammonium_chloride

    Tetramethylammonium chloride is efficiently produced by the reaction of trimethylamine and methyl chloride. [3]N(CH 3) 3 + CH 3 Cl → N(CH 3) 4 + Cl −. It is produced by the alkylation of ammonium chloride with dimethyl carbonate in the presence of an ionic liquid catalyst.

  5. Metallocene - Wikipedia

    en.wikipedia.org/wiki/Metallocene

    General chemical structure of a metallocene compound, where M is a metal cation. A metallocene is a compound typically consisting of two cyclopentadienyl anions (C 5 H − 5, abbreviated Cp) bound to a metal center (M) in the oxidation state II, with the resulting general formula (C 5 H 5) 2 M. Closely related to the metallocenes are the metallocene derivatives, e.g. titanocene dichloride or ...

  6. Methylphosphonyl dichloride - Wikipedia

    en.wikipedia.org/wiki/Methylphosphonyl_dichloride

    Methylphosphonyl dichloride (DC) or dichloro is an organophosphorus compound. It has commercial application in oligonucleotide synthesis, [1] but is most notable as being a precursor to several chemical weapons agents. It is a white crystalline solid that melts slightly above room temperature. [2]

  7. Methylbismuth dichloride - Wikipedia

    en.wikipedia.org/wiki/Methylbismuth_dichloride

    Methylbismuth dichloride is the organobismuth compound with the formula CH 3 BiCl 2. It is a pale yellow solid. The compound can be prepared in two steps from diphenylbismuth chloride, first by methylation with methylmagnesium chloride. Treatment of the resulting methyldiphenylbismuthine with hydrogen chloride cleaves the two phenyl-bismuth bonds.

  8. Dimethyldichlorosilane - Wikipedia

    en.wikipedia.org/wiki/Dimethyldichlorosilane

    Dimethyldichlorosilane hydrolyzes to form linear and cyclic silicones, compounds containing Si-O backbones.The length of the resulting polymer is dependent on the concentration of chain ending groups that are added to the reaction mixture.

  9. Dichlorotris(triphenylphosphine)ruthenium(II) - Wikipedia

    en.wikipedia.org/wiki/Dichlorotris(triphenylp...

    RuCl 2 (PPh 3) 3 is the product of the reaction of ruthenium trichloride trihydrate with a methanolic solution of triphenylphosphine. [1] [2] 2 RuCl 3 (H 2 O) 3 + 7 PPh 3 → 2 RuCl 2 (PPh 3) 3 + 2 HCl + 5 H 2 O + OPPh 3. The coordination sphere of RuCl 2 (PPh 3) 3 can be viewed as either five-coordinate or octahedral.