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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. 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 ...

  4. 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 ...

  5. Biomimetic synthesis - Wikipedia

    en.wikipedia.org/wiki/Biomimetic_synthesis

    Biomimetic synthesis is an area of organic chemical synthesis that is specifically biologically inspired. The term encompasses both the testing of a "biogenetic hypothesis" (conjectured course of a biosynthesis in nature) through execution of a series of reactions designed to parallel the proposed biosynthesis, as well as programs of study where a synthetic reaction or reactions aimed at a ...

  6. 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.

  7. Cascade reaction - Wikipedia

    en.wikipedia.org/wiki/Cascade_reaction

    Cascade reactions are often key steps in the efficient total synthesis of complex natural products. The key step in Heathcock's synthesis of dihydroprotodaphniphylline features a highly efficient cascade involving two aldehyde/amine condensations, a Prins-like cyclization, and a 1,5-hydride transfer to afford a pentacyclic structure from an acyclic starting material.

  8. Synthetic biology - Wikipedia

    en.wikipedia.org/wiki/Synthetic_biology

    [231] [232] Synthetic biology is an example of a dual-use technology with the potential to be used in ways that could intentionally or unintentionally harm humans and/or damage the environment. Often "scientists, their host institutions and funding bodies" consider whether the planned research could be misused and sometimes implement measures ...

  9. Synthetic molecular motor - Wikipedia

    en.wikipedia.org/wiki/Synthetic_molecular_motor

    Synthetic molecular motors are molecular machines capable of continuous directional rotation under an energy input. [2] Although the term "molecular motor" has traditionally referred to a naturally occurring protein that induces motion (via protein dynamics), some groups also use the term when referring to non-biological, non-peptide synthetic motors.

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