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| TriMethyl(broModifluoroMethyl)silane Basic information |
| Product Name: | TriMethyl(broModifluoroMethyl)silane | | Synonyms: | (Bromodifluoromethyl)trimethylsilane 98%;TriMethyl(broModifluoroMethyl)silane;(BroModifluoroMethyl)triMethylsilane;Trimethyl(bromodifluoromethyl)silane 97%;Bromodifluoro(trimethylsilyl)methane;(Bromodifluoromethyl);(Bromodifluoromethyl)trimethylsilane >Silane, (bromodifluoromethyl)trimethyl- | | CAS: | 115262-01-6 | | MF: | C4H9BrF2Si | | MW: | 203.1 | | EINECS: | 806-938-4 | | Product Categories: | | Mol File: | 115262-01-6.mol |
| TriMethyl(broModifluoroMethyl)silane Chemical Properties |
| Boiling point | 108°C(lit.) | | density | 1.306 | | refractive index | n/D1.407 | | Fp | 46℃ | | storage temp. | -20°C | | form | liquid | | color | clear | | InChIKey | WDZVWBWAUSUTTO-UHFFFAOYSA-N | | CAS DataBase Reference | 115262-01-6 |
| Risk Statements | 11 | | Safety Statements | 24/25 | | RIDADR | UN 1993C 3 / PGIII | | TSCA | No | | HazardClass | 3 | | PackingGroup | II | | HS Code | 29319090 |
| TriMethyl(broModifluoroMethyl)silane Usage And Synthesis |
| Uses | Novel difluorocarbene source for the efficient difluoromethylenation of alkenes/alkynes and difluoromethylation of O-, S-, and N-nucleophiles. | | Uses | Trimethyl(bromodifluoromethyl)silane can be used as neuroactive steroids. | | Uses | As reported by Hu and co-workers, (Bromodifluoromethyl)trimethylsilane is a highly useful reagent for the formation of difluoromethene-containing 3-membered rings and can also difluoromethylate heteroatoms with the assistance of alkaline bases, most effectively KOH. | | General Description | (Bromodifluoromethyl)trimethylsilane (TMSCF2Br) is commonly used as a source to generate dilfluorocarbene. TMSCF3 (Ruppert–Prakash reagent) and BBr3 undergoes fast halogen–exchange reaction to form MSCF2Br. |
| TriMethyl(broModifluoroMethyl)silane Preparation Products And Raw materials |
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