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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 [64] [65] In this type of compound sulfur has been replaced by oxygen, selenium and tellurium.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.
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.
It is unclear why trifluralin's exotic 4-trifluoromethyl was tested so early (1960), before more common candidates such as fluoro, bromo, or iodo. [7] By 1968, trifluralin was internationally available, including Australia and New Zealand, [6] and trifluralin was the 5th most used herbicide in the US, at 22,960,000 pounds (10,410 t) by 1974. [11]
Fluazifop is the common name used by the ISO [3] for an organic compound that is used as a selective herbicide. [4] The active ingredient is the 2R enantiomer at its chiral centre and this material is known as fluazifop-P when used in that form. More commonly, it is sold as its butyl ester, fluazifop-P butyl with the brand name Fusilade
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]
Pages in category "Trifluoromethyl compounds" The following 200 pages are in this category, out of approximately 420 total. ... By using this site, you agree to the ...