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  2. Chlorosilane - Wikipedia

    en.wikipedia.org/wiki/Chlorosilane

    In inorganic chemistry, chlorosilanes are a group of reactive, chlorine-containing chemical compounds, related to silane (SiH 4) and used in many chemical processes. Each such chemical has at least one silicon-chlorine (Si−Cl) bond. Trichlorosilane is produced on the largest scale. The parent chlorosilane is silicon tetrachloride (SiCl 4). [1]

  3. Methyltrichlorosilane - Wikipedia

    en.wikipedia.org/wiki/Methyltrichlorosilane

    Methyltrichlorosilane, also known as trichloromethylsilane, is a monomer and organosilicon compound with the formula CH 3 SiCl 3. It is a colorless liquid with a sharp odor similar to that of hydrochloric acid. As methyltrichlorosilane is a reactive compound, it is mainly used a precursor for forming various cross-linked siloxane polymers.

  4. tert-Butyldimethylsilyl chloride - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyldimethylsilyl...

    tert-Butyldimethylsilyl chloride is an organosilicon compound with the formula (Me 3 C)Me 2 SiCl (Me = CH 3). It is commonly abbreviated as TBSCl or TBDMSCl. It is a chlorosilane containing two methyl groups and a tert-butyl group. As such it is more bulky that trimethylsilyl chloride. It is a colorless or white solid that is soluble in many ...

  5. Trimethylsilyl chloride - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilyl_chloride

    TMSCl is reactive toward nucleophiles, resulting in the replacement of the chloride. In a characteristic reaction of TMSCl, the nucleophile is water, resulting in hydrolysis to give the hexamethyldisiloxane: + + The related reaction of trimethylsilyl chloride with alcohols can be exploited to produce anhydrous solutions of hydrochloric acid in alcohols, which find use in the mild synthesis of ...

  6. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    Alkyl groups that contain one ring have the formula −C n H 2n−1, e.g. cyclopropyl and cyclohexyl. The formula of alkyl radicals are the same as alkyl groups, except the free valence "−" is replaced by the dot "•" and adding "radical" to the name of the alkyl group (e.g. methyl radical •CH 3).

  7. Methylsilane - Wikipedia

    en.wikipedia.org/wiki/Methylsilane

    Methylsilane is the organosilicon compound with the formula CH 3 SiH 3. It is a colorless gas that ignites in air. It can be prepared by reduction of methyltrichlorosilane with lithium aluminium hydride. [2] It has been investigated as a precursor to silicon carbide. [3] Methylsilane has been the subject of extensive theoretical analysis. [4]

  8. Category:Organochlorosilanes - Wikipedia

    en.wikipedia.org/wiki/Category:Organochlorosilanes

    For inorganic silicon-hydrogen-chlorine compounds with the general formula Si n H 2n+2-x Cl x, see Category:Chlorosilanes. This category is for organic derivatives of chlorosilanes, where one or more hydrogens have (formally) been replaced by organic groups.

  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. Its structure, including bond lengths and bond angles, has been determined using Fourier transform microwave ...

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