Its applications include the synthesis of specific core scaffolds like 2,6-difluorobenzenesulfonamide and benzoxathiazocine 1,1-dioxides. It is a reactive compound due to the sulfonyl chloride group and the presence of fluorine atoms, but it is also corrosive and requires careful handling. 2,6-Difluorobenzenesulfonyl chloride serves as a reagent in organic synthesis to create sulfonamides and other sulfonyl derivatives, particularly for pharmaceuticals and agrochemicals.
2,6-Difluorobenzenesulfonyl chloride
| API Name | Dabrafenib |
|---|---|
| CAS No | 60230-36-6 |
| Molecular Formula | C6H3ClF2O2S |
| Molecular Weight | 212.60 g/mol |
| Synonyms | 2,6-difluorobenzenesulfonyl chloride |
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Frequently Asked Questions
Its applications include the synthesis of specific core scaffolds like 2,6-difluorobenzenesulfonamide and benzoxathiazocine 1,1-dioxides. It is a reactive compound due to the sulfonyl chloride group and the presence of fluorine atoms, but it is also corrosive and requires careful handling. 2,6-Difluorobenzenesulfonyl chloride serves as a reagent in organic synthesis to create sulfonamides and other sulfonyl derivatives, particularly for pharmaceuticals and agrochemicals.
The CAS number of 2,6-Difluorobenzenesulfonyl chloride is 60230-36-6.
The molecular formula of 2,6-Difluorobenzenesulfonyl chloride is C6H3ClF2O2S.
The listed molecular weight of 2,6-Difluorobenzenesulfonyl chloride is 212.60 g/mol.
2,6-Difluorobenzenesulfonyl chloride is listed as being used in connection with the following API: Dabrafenib.
The listed synonym or IUPAC name for 2,6-Difluorobenzenesulfonyl chloride is 2,6-difluorobenzenesulfonyl chloride.