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Its pK a value in water cannot be accurately determined but in acetonitrile it has been estimated as −0.10 and in 1,2-dichloroethane −12.3 (relative to the pK a value of 2,4,6-trinitrophenol (picric acid), anchored to zero to crudely approximate the aqueous pK a scale [2]), making it more acidic than triflic acid (pK a MeCN = 0.70, pK a DCE ...
In organic chemistry, the triflyl group (systematic name: trifluoromethanesulfonyl group) is a functional group with the formula R−SO 2 CF 3 and structure R−S(=O) 2 −CF 3. The triflyl group is often represented by –Tf. The related triflate group (trifluoromethanesulfonate) has the formula R−OSO 2 CF 3, and is represented by –OTf. [1]
In organic chemistry, triflate (systematic name: trifluoromethanesulfonate), is a functional group with the formula R−OSO 2 CF 3 and structure R−O−S(=O) 2 −CF 3. The triflate group is often represented by −OTf, as opposed to −Tf, which is the triflyl group, R−SO 2 CF 3. For example, n-butyl triflate can be written as CH 3 CH 2 CH ...
Contrary to the popular belief, the CF 3 anion, with [K(18-crown-6)] + as a countercation, was produced and characterized by Prakash and coworkers. [55] The challenges associated with observation of CF 3 anion are alluded to its strong basic nature and its tendency to form pentacoordinated silicon species, such as [Me 3 Si(CF 3) 2] − or [Me 3 ...
Wastewater plants are failing to remove a group of potentially toxic chemicals before pumping treated water into rivers and lakes — and climate change may be making the situation even worse, a ...
Ditolylguanidine is a sigma receptor agonist. [1] It is somewhat [2] selective for sigma receptors, but non-selective between the two sigma receptor subtypes, binding to both σ1 and σ2 with equal affinity. [3] It has neuroprotective [4] and antidepressant effects, [5] and potentiates the effects of NMDA antagonists. [6]
Updated December 28, 2024 at 1:40 PM / Getty Images Manufacturers of baby powder and cosmetic products made with talc will have to test them for asbestos under a proposal announced by the U.S ...
The tert-butyloxycarbonyl protecting group or tert-butoxycarbonyl protecting group [1] (BOC group) is an acid-labile protecting group used in organic synthesis. The BOC group can be added to amines under aqueous conditions using di- tert -butyl dicarbonate in the presence of a base such as sodium hydroxide :