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Sodium trifluoromethanesulfonate

ALDRICH/367907 - 98%

Synonym: Sodium triflate; Trifluoromethanesulfonic acid sodium salt

CAS Number: 2926-30-9
Empirical Formula (Hill Notation): CF3NaO3S
Molecular Weight: 172.06
MDL Number: MFCD00061607
Linear Formula: CF3SO3Na
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-367907-5G 5 g
$74.20
1/EA
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45-367907-25G 25 g
$226.00
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 367907-25G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 367907-5G

 

assay 98%
form solid
InChI 1S/CHF3O3S.Na/c2-1(3,4)8(5,6)7;/h(H,5,6,7);/q;+1/p-1
InChI key XGPOMXSYOKFBHS-UHFFFAOYSA-M
mp 253-255 °C (lit.)
SMILES string [Na+].[O-]S(=O)(=O)C(F)(F)F
Application: Sodium trifluoromethanesulfonate can be employed as a reagent for the preparation of:
• Aryl fluorides via silver-catalyzed fluorination of arylstannanes.
• Ionic liquids such as N, N -dialkylpyrrolidinium triflate, N,N-dialkylimidazolium triflate, and N-alkylpyridinium triflate.

It can be also used as supporting electrolyte in electrochemical O-glycosylation of primary alcohols with O-protected thioglycosides.
General description: Sodium trifluoromethanesulfonate (Sodium triflate or NaOTf) is an efficient catalyst as well as a reagent in many organic reactions. The prominent application includes catalytic asymmetric Mannich-type reactions, Mannich-type reactions in water, and Diels-Alder reactions.It is also used as an electrolyte in batteries.
Packaging: 5, 25 g in glass bottle
Purity 98%
mp 253-255 °C (lit.)
UNSPSC 12352302

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