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  2. Trifluoromethylation - Wikipedia

    en.wikipedia.org/wiki/Trifluoromethylation

    The reagent was used in trifluoromethylation of a thiophenolate. S-(trifluoromethyl)dibenzothiophenium tetrafluoroborate is a commercially available and known trifluoromethylation reagent based on the same principle first documented in 1990. [64] [65] In this type of compound sulfur has been replaced by oxygen, selenium and tellurium.

  3. Trifluoromethyl group - Wikipedia

    en.wikipedia.org/wiki/Trifluoromethyl_group

    Sulfoxaflor is used as a systemic insecticide. Trifluralin, as with several dinitritroaniline herbicides, is a trifluoromethyl herbicide. Fluazifop is another, a phenoxy herbicide. The trifluoromethyl group can also be added to change the solubility of molecules containing other groups of interest.

  4. Trifluoromethyltrimethylsilane - Wikipedia

    en.wikipedia.org/wiki/Trifluoromethyltrimethylsilane

    Trifluoromethyltrimethylsilane (known as Ruppert-Prakash reagent, TMSCF 3) is an organosilicon compound with the formula CF 3 Si(CH 3) 3.It is a colorless liquid. The compound is a reagent used in organic chemistry for the introduction of the trifluoromethyl group.

  5. Trifluorotoluene - Wikipedia

    en.wikipedia.org/wiki/Trifluorotoluene

    A second and perhaps more valuable use of trifluorotoluene is as a synthetic intermediate. A derivative of trifluorotoluene, 3-aminobenzotrifluoride, is the precursor to the herbicide fluometuron. [3] It is synthesized via nitration followed by reduction to meta-H 2 NC 6 H 4 CF 3. This aniline is then converted to the urea.

  6. Trifluoroiodomethane - Wikipedia

    en.wikipedia.org/wiki/Trifluoroiodomethane

    Trifluoroiodomethane, also referred to as trifluoromethyl iodide is a halomethane with the formula CF 3 I. It is an experimental alternative to Halon 1301 (CBrF 3 ) in unoccupied areas. [ 1 ] It would be used as a gaseous fire suppression flooding agent for in-flight aircraft and electronic equipment fires.

  7. Trifluoromethanol - Wikipedia

    en.wikipedia.org/wiki/Trifluoromethanol

    A simpler synthesis uses the reaction (I); an equilibrium can be shifted to the thermodynamically preferred trifluoromethanol at lower temperatures. If the synthesized trifluoromethanol is protonated by superacids, for example HSbF 6 (fluoroantimonic acid), the equilibrium can be further shifted to the left towards the desired product.

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  9. Trifluoromethyl cation - Wikipedia

    en.wikipedia.org/wiki/Trifluoromethyl_cation

    The trifluoromethyl cation is a molecular cation with a formula of CF + 3. It is a carbocation due to its positively charged carbon atom. It is part of the family of carbenium ions, with three fluorine atoms as substituents in place of its hydrogen atoms. [1]