1,3-dibromo-2-fluoro-5-nitrobenzene
$250.00
CAS No.: 361436-26-2
Catalog No.: WLZ1571
Purity: 95%
MF: C6H2Br2FNO2
MW: 298.893
Storage: 2-8 degree Celsius
SMILES: BrC1=C(C(=CC(=C1)[N+](=O)[O-])Br)F
Catalog No.: WLZ1571
Purity: 95%
MF: C6H2Br2FNO2
MW: 298.893
Storage: 2-8 degree Celsius
SMILES: BrC1=C(C(=CC(=C1)[N+](=O)[O-])Br)F
CAS NO.: 361436-26-2; 1,3-dibromo-2-fluoro-5-nitrobenzene. PROPERTIES: This nitrohalogenated aromatic compound features two bromine atoms, a fluorine atom, and a nitro group on a benzene ring, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The 1,3-dibromo-2-fluoro-5-nitrobenzene typically appears as a white crystalline powder with limited aqueous solubility but good solubility in common organic solvents. Its molecular structure includes multiple halogen atoms and a nitro group that influence the electronic properties of the aromatic system. For optimal stability and to prevent degradation, this compound should be stored at 2-8 degree Celsius in a tightly sealed container under anhydrous conditions. When handling, appropriate safety measures including nitrile gloves and safety goggles are essential. This compound is sensitive to moisture and may hydrolyze in aqueous environments. In case of accidental spillage, clean the area with a damp cloth and dispose of materials according to local regulations. APPLICATIONS: The 1,3-dibromo-2-fluoro-5-nitrobenzene serves as a valuable intermediate in the synthesis of highly functionalized aromatic compounds and materials with specific electronic properties. The bromine substituents provide handles for cross-coupling reactions, enabling the creation of substituted benzene derivatives with diverse biological activities. In medicinal chemistry, this compound functions as a building block for developing pharmaceuticals targeting enzyme inhibitors and receptor modulators. The nitro group can be further reduced to amine functionality for additional diversification. Additionally, the molecule finds utility in materials science as a monomer for creating polymers with specific electronic and optical properties. Researchers utilizing this compound benefit from its defined halogenation pattern and functional group arrangement, enabling the development of advanced materials with tailored electronic characteristics.
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