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| 1-(Fluorosulfuryl)-2,3- Basic information |
| Product Name: | 1-(Fluorosulfuryl)-2,3- | | Synonyms: | 1-(Fluorosulfuryl)-2,3-;1-(fluorosulfonyl)-2,3-dimethyl-1H-imidazol-3-ium trifluoromethanesulfonate;1-(Fluorosulfonyl)-2-dimethyl-1H-imidazol-3-ium trifluoromethanesulfonate;185051;7-bromo-5-methyl-1,2,3,4-tetrahydroisoquinoline1-(Fluorosulfonyl)-2,3-dimethyl-1H-imidazol-3-ium trifluoromethanesulfonate;1-(Fluorosulfuryl)-2,3-dimethyl-1H-imidazol-3-ium trifluoromethanesulfonate;3-(Fluorosulfonyl)-1,2-dimethyl-1H-imidazol-3-ium trifluoromethanesulfonate | | CAS: | 2179072-33-2 | | MF: | C6H8F4N2O5S2 | | MW: | 328.25 | | EINECS: | | Product Categories: | | Mol File: | 2179072-33-2.mol |
| 1-(Fluorosulfuryl)-2,3- Chemical Properties |
| Melting point | 64-65 °C | | storage temp. | 2-8°C |
| 1-(Fluorosulfuryl)-2,3- Usage And Synthesis |
| Uses | This solid fluorosulfuryl imidazolium triflate salt, SuFEx-IT, is a convenient alternative to sulfuryl fluoride (SO2F2), which is a harmful fumigant gas with difficult handling procedures that make SO2F2 -- and the products it is capable of making -- difficult to access. However, this reagent possesses novel reactivity, selectivity, and scope and was demonstrated by the labs of K. Barry Sharpless and Jiajia Dong to convert phenols, primary amines, and secondary amines to fluorosulfates and sulfamoyl fluorides. Fluorosulfates are used widely in biological studies, medicinal chemistry, and work as a pseudohalide in Pd-catalysed cross-coupling reactions. Store in dry environment (desiccator advised) at 4 °C. |
| 1-(Fluorosulfuryl)-2,3- Preparation Products And Raw materials |
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