Introduction：Basic information about MAGNESIUM TRIFLUOROMETHANESULFONIMIDE CAS 133395-16-1, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
MAGNESIUM TRIFLUOROMETHANESULFONIMIDE Basic informationReaction
| 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: | 209-622-9 |
| Product Categories: | OTf&NTf series;Other Metal |
| Mol File: | 133395-16-1.mol |
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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 |
| Major Application | battery manufacturing |
| InChI | InChI=1S/2C2F6NO4S2.Mg/c2*3-1(4,5)14(10,11)9-15(12,13)2(6,7)8;/q2*-1;+2 |
| InChIKey | DMFBPGIDUUNBRU-UHFFFAOYSA-N |
| SMILES | C(S1([N-]S(=O)(C(F)(F)F)=O[Mg+2]2(O=S(=O)(C(F)(F)F)[N-]S(=O)(C(F)(F)F)=O2)O=1)=O)(F)(F)F |
Safety Information
| Hazard Codes | C |
| Risk Statements | 34 |
| Safety Statements | 22-26-36/37/39-45 |
| RIDADR | UN 1759 8 / PGII |
| WGK Germany | 3 |
| HS Code | 2935.90.9500 |
| HazardClass | 8 |
| PackingGroup | II |
| Storage Class | 8A - Combustible corrosive hazardous materials |
| Hazard Classifications | Skin Corr. 1B |
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.
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| 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
| Preparation Products | BENZYL ETHYL ETHER |
