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[5] [6] FTOHs can also be used as intermediates in the production of surfactants. [7] Fluorotelomer alcohols can biodegrade to perfluorinated carboxylic acids, which persist in the environment and are found in the blood serum of populations and wildlife, such as the toxic PFOA and PFNA. [8] [9] Aerobic biotransformation pathways of 8:2 FTOH in ...
Fluoroalcohol. 3 languages. 日本語 ... [1] Perfluoroalcohols. Most primary and secondary perfluoroalcohols are unstable, for example trifluoromethanol eliminates ...
Pentafluorophenol is the organofluorine compound (specifically a fluoroalcohol) with the formula C 6 F 5 OH. This is the perfluorinated analogue of phenol. It is a white solid that melts just above room temperature, and smells of phenol. With a pK a of 5.5, it is one of the most acidic phenols.
Nonafluoro-tert-butyl alcohol (IUPAC name: 1,1,1,3,3,3-hexafluoro-2-(trifluoromethyl)propan-2-ol) is a fluoroalcohol. It is the perfluorinated analog of tert -butyl alcohol . Notably, as a consequence of its electron withdrawing fluorine substituents, it is very acidic for an alcohol, with a p K a value of 5.4, similar to that of a carboxylic acid.
This page is the template for the metabolic pathways template. This template should be used to illustrate the general 'shape' of metabolism within the cell . This template is part of the Metabolic Pathways task force .
It is classified as a hard Lewis acid and its acceptor properties are discussed in the ECW model yielding E A = 2.07 and C A = 1.06. TFE can be used in biochemical experiments to stabilize alpha helix. [7] [8] There are also stable beta sheets in TFE, suggesting that TFE stabilizes the secondary structure the sequence has a preference for. [8]
Trifluoroacetaldehyde, trifluoroethanal, or fluoral, [2] is a fluorinated derivative of acetaldehyde with the formula CF 3 CHO.It is a gas at room temperature. Fluoral is used to introduce trifluoromethyl groups into organic compounds.
2-Fluoroethanol was originally synthesized by treating 2-chloroethanol with potassium fluoride, in a simple Finkelstein reaction. [5] The product has a lower boiling point that the starting material and may be conveniently isolated by distillation.