2923-28-6
2923-28-6
Chemical Structure
Silver trifluoromethanesulfonate
Synonym(s): Triflic acid silver; Perfluoromethanesulfonic acid silver; Fluorad FC 24 silver
- CAS No.: 2923-28-6
- Formula:CF3SO3Ag
- Molecular Weight:256.94
IUPAC Name: silver(I) trifluoromethanesulfonate
InChIKey: QRUBYZBWAOOHSV-UHFFFAOYSA-M
SMILES: O=S(C(F)(F)F)([O-])=O.[Ag+]
Biological Activity: Silver trifluoromethanesulfonate, a perfluoroalkanesulfonic acid, is one of the superior catalysts for C- or O-acylation. Silver trifluoromethanesulfonate is widely used as a cationic catalyst in promoting Friedel-Crafts reactions and esterification reactions[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Silver trifluoromethanesulfonate | 98.0% | Silver trifluoromethanesulfonate, a perfluoroalkanesulfonic acid, is one of the superior catalysts for C- or O-acylation. Silver trifluoromethanesulfonate is widely used as a cationic catalyst in promoting Friedel-Crafts reactions and esterification reactions. | ||||||||||||||||||||
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References
- [1]. Zetryana Puteri Tachrim, et al. Trifluoromethanesulfonic Acid as Acylation Catalyst: Special Feature for C- and/or O-Acylation Reactions. Catalysts 2017, 7(2), 40.
- [2]. Pertel SS. Silver trifluoromethanesulfonate as a new efficient catalyst for glycosylation reactions using 2-alkoxy-glyco-[2,1-d]-2-oxazoline glycosyl donors, contributing to the suppression of side reactions of intermolecular aglycon transfer and polymerization of oxazoline derivatives of sugars. Carbohydr Res. 2025 Jun;552:109452. [Content Brief]
