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  2. Dimethyldichlorosilane - Wikipedia

    en.wikipedia.org/wiki/Dimethyldichlorosilane

    The main purpose of dimethyldichlorosilane is for use in the synthesis of silicones, an industry that was valued at more than $10 billion per year in 2005. It is also employed in the production of polysilanes, which in turn are precursors to silicon carbide . [ 3 ]

  3. Silanes - Wikipedia

    en.wikipedia.org/wiki/Silanes

    The dominant examples come from the Direct process, i.e., (CH 3) 4-x SiCl x. Another important member is trichlorosilane (SiHCl 3). Organosilanes are a class of charge-neutral organosilicon compounds. Example: tetramethylsilane (Si(CH 3) 4) By tradition, compounds with Si-O-Si bonds are usually not referred to as silanes. Instead, they are ...

  4. Direct process - Wikipedia

    en.wikipedia.org/wiki/Direct_process

    The major product for the direct process should be dichlorodimethylsilane, Me 2 SiCl 2. However, many other products are formed. Unlike most reactions, this distribution is actually desirable because the product isolation is very efficient. [1] Each methylchlorosilane has specific and often substantial applications. Me 2 SiCl 2 is the most ...

  5. Dichlorosilane - Wikipedia

    en.wikipedia.org/wiki/Dichlorosilane

    Stock and Somieski completed the hydrolysis of dichlorosilane by putting the solution of H 2 SiCl 2 in benzene in brief contact with a large excess of water. [3] [5] A large-scale hydrolysis was done in a mixed ether/alkane solvent system at 0 °C, which gave a mixture of volatile and nonvolatile [H 2 SiO] n.

  6. Organosilicon chemistry - Wikipedia

    en.wikipedia.org/wiki/Organosilicon_chemistry

    Although proportionately a minor outlet, organosilicon compounds are widely used in organic synthesis. Notably trimethylsilyl chloride Me 3 SiCl is the main silylating agent. One classic method called the Flood reaction for the synthesis of this compound class is by heating hexaalkyldisiloxanes R 3 SiOSiR 3 with concentrated sulfuric acid and a ...

  7. Chlorosilane - Wikipedia

    en.wikipedia.org/wiki/Chlorosilane

    Other acid-forming species, especially acetate, can replace chlorine in silicone synthesis with little difference in the chemistry of the finished polymer. These analogues of chlorosilanes are quite common in the sealants and adhesives marketed to consumers, and as precursors for medical-grade silicone, because of reduced toxicity.

  8. Silanol - Wikipedia

    en.wikipedia.org/wiki/Silanol

    Structure of trimethylsilanol. A silanol is a functional group in silicon chemistry with the connectivity Si–O–H. It is related to the hydroxy functional group (C–O–H) found in all alcohols.

  9. Chlorodimethylsilane - Wikipedia

    en.wikipedia.org/wiki/Chlorodimethylsilane

    Chlorodimethylsilane, also called dimethylchlorosilane and abbreviated DMCS, is a chemical compound with the formula (CH 3) 2 SiHCl. It is a silane, with a silicon atom bonded to two methyl groups, a chlorine atom, and a hydrogen atom.