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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 [64] [65] In this type of compound sulfur has been replaced by oxygen, selenium and tellurium.
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.
Fluridone's main action to disrupt photosynthesis in plants is by preventing the secretion of abscisic acid. [8] As higher eukaryotes, such as humans, also rely on an abscisic acid pathway [9] to create inflammation in normal physiological processes, fluridone could be investigated as being of interest in the development of anti-inflammatory agents.
An additional stabilization is achieved by the trifluoromethyl group, which acts as a strong electron-withdrawing group using the sulfur atom as a bridge. Triflates have also been applied as ligands for group 11 and 13 metals along with lanthanides. Lithium triflates are used in some lithium ion batteries as a component of the electrolyte.
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.
Trifluralin is a common pre-emergent selective herbicide, a dinitroaniline.With about 14 million pounds (6,400 t) used in the United States in 2001, [3] and 3–7 million pounds (1,400–3,200 t) in 2012, [4] it is one of the most widely used herbicides.
Many organofluorine compounds are generated from reagents that deliver perfluoroalkyl and perfluoroaryl groups. (Trifluoromethyl)trimethylsilane, CF 3 Si(CH 3) 3, is used as a source of the trifluoromethyl group, for example. [24] Among the available fluorinated building blocks are CF 3 X (X = Br, I), C 6 F 5 Br, and C 3 F 7 I.
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.