| Identification | Back Directory | [Name]
3-BROMO-4-NITROPYRIDINE | [CAS]
89364-04-5 | [Synonyms]
IFLAB-BB F1371-0211
3-BROMO-4-NITROPYRIDINE
i3-Bromo-4-nitropyridine
Pyridine, 3-bromo-4-nitro-
3-BROMO-4-NITROPYRIDINE 97%
3-BROMO-4-NITROPYRIDINE ISO 9001：2015 REACH | [Molecular Formula]
C5H3BrN2O2 | [MDL Number]
MFCD03085767 | [MOL File]
89364-04-5.mol | [Molecular Weight]
202.99 |
| Chemical Properties | Back Directory | [Melting point ]
66-67 °C | [Boiling point ]
235.7±20.0 °C(Predicted) | [density ]
1.833±0.06 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [pka]
-1.04±0.18(Predicted) | [InChI]
InChI=1S/C5H3BrN2O2/c6-4-3-7-2-1-5(4)8(9)10/h1-3H | [InChIKey]
CJEWCWSWUUFORD-UHFFFAOYSA-N | [SMILES]
C1=NC=CC([N+]([O-])=O)=C1Br |
| Hazard Information | Back Directory | [Synthesis]
A mixture of 3-bromo-4-nitropyridine N-oxide (2.2g,10 mmol), trichlorooxobis (triphenylphosphine) rhenium(V) [Re(0)(Ph3P)2Cl3, Aldrich, 50 mg, 0.08mmol), and triphenyphosphine (2.7 g, 10.3 mmol) in dichloromethane (100 mL) was flushed with argon and stirred at rt for 1 h, then, at 40 °C for 2 h. The reaction mixture was cooled to rt and concentrated under vacuum. The residue was triturated with hexanes (300 mL), and the precipitated (triphenylphosphine oxide) was removed by filtration. The organic layer was concentrated and purified by column (silica gel, EtOAc/hexanes 1/7) to give 3-Bromo-4-nitropyridine as yellow solid (1.8 g, 86%)[1]. | [References]
[1] R. W. Daisley, J. R. Hanbali. “PREPARATION OF 3-BROMO-4-NITROPYRIDINE 1-OXIDE.” Organic Preparations and Procedures International 15 1 (1983): 280–282. |
|
|