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| | 2-BROMO-4,6-DIFLUORONITROBENZENE Basic information |
| Product Name: | 2-BROMO-4,6-DIFLUORONITROBENZENE | | Synonyms: | 1-broMo-3,5-difluoro-2-nitrobenzene;2-BROMO-4,6-DIFLUORONITROBENZENE;Benzene, 1-bromo-3,5-difluoro-2-nitro-;2-BROMO-4,6-DIFLUORONITROBENZENE ISO 9001：2015 REACH | | CAS: | 884494-38-6 | | MF: | C6H2BrF2NO2 | | MW: | 237.99 | | EINECS: | | | Product Categories: | | | Mol File: | Mol File |  |
| | 2-BROMO-4,6-DIFLUORONITROBENZENE Chemical Properties |
| Boiling point | 226.9±35.0 °C(Predicted) | | density | 1.890±0.06 g/cm3(Predicted) | | storage temp. | Sealed in dry,Room Temperature | | form | crystalline powder | | color | Off-white to faint yellow |
| | 2-BROMO-4,6-DIFLUORONITROBENZENE Usage And Synthesis |
| Uses | 2-Bromo-4,6-difluoronitrobenzene is a polysubstituted fluoronitrobenzene analogue that can be used to prepare pyrazolylamino benzimidazole derivatives as JAK inhibitors. | | Synthesis | Fuming nitric acid (20 mL) was slowly added dropwise to a solution of 1-bromo-3,5-difluorobenzene (35.00 mL, 304 mmol) dissolved in sulfuric acid (50 mL) at 0 °C. The reaction mixture was slowly warmed to room temperature and stirred overnight. The reaction mixture was carefully poured into an ice-water mixture (600 mL) and subsequently slowly warmed to room temperature. Ethyl acetate (200 mL) and hexane (100 mL) were added and stirred until all solids were completely dissolved. The organic layer was separated, washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, filtered and concentrated in vacuum to give 2-bromo-4,6-difluoronitrobenzene as a yellow oil (57.37 g, 79% yield).GCMS analysis showed m/z = 237,239 (corresponding to Br isotope pattern). | | References | [1] Journal of Medicinal Chemistry, 2008, vol. 51, # 17, p. 5243 - 5263
[2] Patent: US9556153, 2017, B1. Location in patent: Page/Page column 8
[3] Patent: WO2018/13486, 2018, A1. Location in patent: Page/Page column 13 |
| | 2-BROMO-4,6-DIFLUORONITROBENZENE Preparation Products And Raw materials |
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