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2926-27-4

Methanesulfonic acid, 1,1,1-trifluoro-, potassium salt (1:1)

Catalog#: AR002YK7  |   CAS#: 2926-27-4  |   MDL#: MFCD00042370  |   MF: CF3KO3S  |   MW: 188.1674

Packsize Purity Price Availability Quantity
1g 95% $3.00 Global Stock Buy Now Add To Cart
5g 95% $4.00 Global Stock Buy Now Add To Cart
10g 95% $8.00 Global Stock Buy Now Add To Cart
25g 95% $12.00 Global Stock Buy Now Add To Cart
100g 95% $45.00 Global Stock Buy Now Add To Cart
500g 95% $200.00 Global Stock Buy Now Add To Cart
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Catalog Number AR002YK7
Chemical Name Methanesulfonic acid, 1,1,1-trifluoro-, potassium salt (1:1)
CAS Number 2926-27-4
Molecular Formula CF3KO3S
Molecular Weight 188.1674
MDL Number MFCD00042370
SMILES FC(S(=O)(=O)[O-])(F)F.[K+]

Potassium trifluoromethanesulfonate, also known as CF3SO3K, is a versatile reagent commonly used in chemical synthesis for various applications. This reagent plays a crucial role in organic chemistry as a source of the trifluoromethanesulfonyl (triflyl) group, which can be utilized in a wide range of synthetic transformations.One of the primary applications of Potassium trifluoromethanesulfonate is as a source of the triflyl cation in reactions involving carbocations. The triflyl group is known for its ability to stabilize carbocation intermediates, making it a valuable tool in organic synthesis for the formation of carbon-carbon bonds. This reagent is often used in reactions such as Friedel-Crafts alkylations and cyclizations to facilitate the generation of carbocation species.Additionally, Potassium trifluoromethanesulfonate is commonly employed as a mild and selective fluorinating agent in organic synthesis. The triflyl group can be easily substituted by fluoride ions, leading to the introduction of a fluorine atom into organic molecules. This fluoroalkylation reaction is particularly useful in the preparation of fluorinated organic compounds, which are important in pharmaceuticals, agrochemicals, and materials science.Furthermore, Potassium trifluoromethanesulfonate can act as a powerful acid catalyst in various transformations, such as esterifications, acylations, and rearrangements. The strong acidity of the triflyl group makes it an effective catalyst for promoting these reactions under mild conditions, enabling the efficient synthesis of a wide range of organic compounds.In summary, Potassium trifluoromethanesulfonate is a valuable reagent in chemical synthesis, offering a versatile platform for the introduction of the triflyl group and fluorine atoms into organic molecules, as well as serving as an effective acid catalyst in various transformations.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H315-H319
Precautionary Statements P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class -
Packing Group -

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