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| MAGNESIUM TRIFLUOROMETHANESULFONIMIDE Basic information | | Reaction |
| Product Name: | MAGNESIUM TRIFLUOROMETHANESULFONIMIDE | | Synonyms: | MAGNESIUM TRIFLUOROMETHANESULFONIMIDE;Magnesium bis(trifluoromethylsulfonyl)imide, min. 97%;MagnesiuM bis(trifluoroMethylsulfonyl)iMide;Magnesium trifluoromethanesulfonamide;Magnesium bis(trifluoromethanesulfonimide);Magnesium(II) Bis(trifluoromethanesulfonyl)imide;Magnesium bis[bis[(trifluoromethyl)sulfonyl]amide;Mg[(CF3SO2)2N]2MgTFSI | | CAS: | 133395-16-1 | | MF: | C4F12MgN2O8S4 | | MW: | 584.6 | | EINECS: | | Product Categories: | OTf&NTf series;Other Metal | | Mol File: | 133395-16-1.mol |
| MAGNESIUM TRIFLUOROMETHANESULFONIMIDE Chemical Properties |
| Melting point | >200℃ | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | form | Powder | | color | white | | Water Solubility | Insoluble in water. | | Sensitive | Moisture Sensitive |
| Hazard Codes | C | | Risk Statements | 34 | | Safety Statements | 22-26-36/37/39-45 | | RIDADR | UN 1759 8 / PGII | | WGK Germany | 3 | | HazardClass | 8 | | PackingGroup | II |
| MAGNESIUM TRIFLUOROMETHANESULFONIMIDE Usage And Synthesis |
| Reaction |
- Useful catalyst for the Diels-Alder reaction.
- Efficient catalyst for the nucleophilic substitution of allylic and benzylic acetates.
- Catalyst used in the acylation of phenols, alcohols, and thiols with anhydrides.
- Catalyst in asymmetric radical additions to olefins.
- Catalyst in the enantioselective 1,3-Dipolar Cycloaddition of diazoacetates and olefins.
- Precatalyst for enantioselective synthesis of isoxazolidinones.
| | Uses | Magnesium bis(trifluoromethylsulfonyl)imide is a strong Lewis acid and used as a catalyst in organic synthesis. It is an electrolyte, which shows high anodic stability used in rechargeable magnesium batteries. |
| MAGNESIUM TRIFLUOROMETHANESULFONIMIDE Preparation Products And Raw materials |
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