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| | Sodium trifluoromethanesulfonate Basic information |
| Product Name: | Sodium trifluoromethanesulfonate | | Synonyms: | SODIUM TRIFLATE;SODIUM TRIFLATE TRIFLUOROMETHANESULFONIC ACID, SODIUM SALT;SODIUM TRIFLUOROMETHANESULFONATE;SODIUM TRIFLUOROMETHANESULPHONATE;TRIFLUOROMETHANESULFONIC ACID SODIUM SALT;SodiuM trifluoroMethanesulfonate, 98% 5GR;Sodium trifluoromethanesulphonate 98%;Sodiumtrifluoromethanesulphonate98% | | CAS: | 2926-30-9 | | MF: | CF3NaO3S | | MW: | 172.06 | | EINECS: | | | Product Categories: | triflate | | Mol File: | 2926-30-9.mol |  |
| | Sodium trifluoromethanesulfonate Chemical Properties |
| Melting point | 253-255 °C (lit.) | | storage temp. | Inert atmosphere,Room Temperature | | form | Powder | | color | White to off-white | | Water Solubility | soluble | | Sensitive | Hygroscopic | | Hydrolytic Sensitivity | 0: forms stable aqueous solutions | | BRN | 3728797 | | InChIKey | KKVTYAVXTDIPAP-UHFFFAOYSA-M | | CAS DataBase Reference | 2926-30-9(CAS DataBase Reference) |
| | Sodium trifluoromethanesulfonate Usage And Synthesis |
| Chemical Properties | White to off-white powder | | Uses | Sodium trifluoromethanesulfonate is used in the preparation of N-fluoro-2-methylpyridinium triflate by reaction with dinitrogen difluoride as a reagent. It is also used as a chaotropic mobile phase additive in reversed-phase liquid chromatography (RP-LC). | | Uses | 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. |
| | Sodium trifluoromethanesulfonate Preparation Products And Raw materials |
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