CAS: 358-23-6 Trifluoromethanesulfonic anhydride
Product Name: Trifluoromethanesulfonic anhydride
Synonyms: Trifluoromethanesulfonic anhydlladium(0);Trifluoromethanesulfonic anhydride purum, >=98.0% (T);Trifluoromethanesulfonic anhydride solution 1 M in methylene chloride;Triflic anhydride solution;7561347, DT: 23.1 1.2016) RE-EXPORT;TRIFLUOROMETHANE SULFONIC ANHYDRIDE(ORIG INAL IMPORT VIDE BE.NO;Trifluoromethanesulfonic anhydride solution ;Methanesulfonic acid, trifluoro-, anhydride
CAS: 358-23-6
MF: C2F6O5S2
MW: 282.14
EINECS: 206-616-8
Product Categories: organofluorine compounds;Pharmaceutical intermediates;pharmacetical;Organic Fluorides
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Description Trifluoromethanesulfonic anhydride, also known as triflic anhydride, has proven to be an extraordinary reagent for a broad range of transformations. As a commercially and readily available reagent, It has been widely used in synthetic chemistry due to its high electrophilicity. Given its high affinity towards O-nucleophiles, reaction with alcohols, carbonyls, sulfur phosphorus- and iodine oxides towards the formation of the corresponding triflates is strongly favored. As one of the premier leaving groups in organic chemistry, the generated triflates then open the door to various downstream transformations, including (but not limited to) substitution reactions, cross-coupling processes, redox reactions, and rearrangements[1-2].
Uses Trifluoromethanesulfonic Anhydride is a strong electrophile used in chemical synthesis for introducing the triflyl group.
Uses Trifluoromethanesulfonic anhydride is used to convert phenols and imine into triflic ester and NTf group. It is a strong electrophile used for the introduction of triflyl group in chemical synthesis. It serves as a reagent in the preparation of alkyl and vinyl triflates, and for the stereoselective synthesis of mannosazide methyl uronate donors. It acts as a catalyst for glycosylation with anomeric hydroxy sugars to prepare polysaccharides."
Chemical Properties clear colorless to light brown liquid
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