- 2,5-Dibromo-3-nitropyridine
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- $6.00 / 1KG
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2024-04-05
- CAS:15862-37-0
- Min. Order: 1KG
- Purity: 98%
- Supply Ability: g-kg-tons, free sample is available
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| | 2,5-Dibromo-3-nitropyridine Basic information |
| Product Name: | 2,5-Dibromo-3-nitropyridine | | Synonyms: | 2,5-Dibromo-3-nitropyridine;Nsc170627;2,5-Dibromo-3-nitropyridine ,97%;2,5-Dibromo-3-nitropyridi...;Pyridine,2,5-dibroMo-3-nitro-;2,5-DibroMo-3-nitro-pyridine;2,5-Dibromo-3-nitropyridine >;2,5-Dibromo-3-nitropyridine,98% | | CAS: | 15862-37-0 | | MF: | C5H2Br2N2O2 | | MW: | 281.89 | | EINECS: | 808-084-8 | | Product Categories: | Thiazines ,Thiazoles;Pyridines;Heterocyclic Compounds;Pyridine series;Pyridine | | Mol File: | 15862-37-0.mol |  |
| | 2,5-Dibromo-3-nitropyridine Chemical Properties |
| Melting point | 92.0 to 96.0 °C | | Boiling point | 272.7±35.0 °C(Predicted) | | density | 2?+-.0.06 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | | solubility | soluble in Methanol | | pka | -5.60±0.20(Predicted) | | form | Solid | | color | Yellow | | InChIKey | OQKWPJCAKRVADO-UHFFFAOYSA-N | | CAS DataBase Reference | 15862-37-0(CAS DataBase Reference) |
| Hazard Codes | Xi,T | | Risk Statements | 25 | | Safety Statements | 45 | | RIDADR | UN 2811 6.1 / PGIII | | WGK Germany | 3 | | HazardClass | IRRITANT | | HS Code | 2933399990 |
| | 2,5-Dibromo-3-nitropyridine Usage And Synthesis |
| Uses | 2,5-Dibromo-3-nitropyridine is used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process. | | Preparation | synthesis of 2,5-Dibromo-3-nitropyridine: To a suspension 5-bromo-3-nitro-pyridin-2-ol (20 g, 91.32 mmol) in toluene (100 ml) was added DMF (0.7 ml, 9.13 mmol) and the mixture was heated to 90??C. (the reaction mixture was protected from light). A solution of POBr3 (31. 41 g, 109.51 mmol) in toluene (40 ml) was added dropwise at 90??C. and the reaction mixture was stirred at that temperature for 16 h. The mixture was allowed to cool to room temperature and toluene (50 ml) and water (50 ml) were added. The organic layer was separated, washed successively with aqueous 1N NaOH (60 ml), water (60 ml) and brine (30 ml), dried with Na2SO4 and evaporated obtain 2,5-Dibromo-3-nitropyridine. Yellow solid, yield 25.2 g, 97%.
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| | 2,5-Dibromo-3-nitropyridine Preparation Products And Raw materials |
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