| Identification | Back Directory | [Name]
1-Bromo-3-fluoro-2-nitrobenzene | [CAS]
886762-70-5 | [Synonyms]
2-fluoro-6-bromonitrobenzene
1-Bromo-3-fluoro-2-nitrobenzene
2-Bromo-6-fluoronitrobenzene 97%
Benzene, 1-bromo-3-fluoro-2-nitro-
1-Bromo-3-fluoro-2-nitrobenzene >
1-Bromo-3-fluoro-2-nitrobenzene ISO 9001：2015 REACH | [EINECS(EC#)]
689-316-3 | [Molecular Formula]
C6H3BrFNO2 | [MDL Number]
MFCD07368788 | [MOL File]
886762-70-5.mol | [Molecular Weight]
220 |
| Chemical Properties | Back Directory | [Melting point ]
36-37°C | [Boiling point ]
232.0±20.0 °C(Predicted) | [density ]
1.808±0.06 g/cm3(Predicted) | [Fp ]
87° | [storage temp. ]
Sealed in dry,2-8°C | [solubility ]
soluble in Methanol | [form ]
powder to lump | [color ]
White to Orange to Green | [InChI]
InChI=1S/C6H3BrFNO2/c7-4-2-1-3-5(8)6(4)9(10)11/h1-3H | [InChIKey]
VFPAOFBPEYCAAZ-UHFFFAOYSA-N | [SMILES]
C1(Br)=CC=CC(F)=C1[N+]([O-])=O |
| Hazard Information | Back Directory | [Chemical Properties]
light yellow crystalline powder | [Uses]
2-Bromo-6-fluoronitrobenzene is a hydrocarbon derivative, mainly used as an organic intermediate.
| [Reactions]
The structure of 2-bromo-6-fluoronitrobenzene contains a nitro unit with high electron-withdrawing properties, which can easily undergo aromatic nucleophilic substitution reactions under the attack of common nucleophiles such as alcohols or amines. | [Synthesis]
To a suspension of sodium perborate tetrahydrate (135.374 g., 886.4 mmol) in 500 mL of acetic acid at 55°C was added dropwise
2-bromo-6-fluoroaniline (33.685 g., 177.271 mmol) in 70 mL
solution in acetic acid. The reaction mixture was stirred at 55° C. |
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