2-bromo-4-fluoro-1-nitro-3-(trifluoromethyl)benzene
$150.00
CAS No.: 1805937-67-0
Catalog No.: WLZ1630
Purity: 95%
MF: C7H2BrF4NO2
MW: 287.994
Storage: 2-8 degree Celsius
SMILES: BrC1=C(C=CC(=C1C(F)(F)F)F)[N+](=O)[O-]
Catalog No.: WLZ1630
Purity: 95%
MF: C7H2BrF4NO2
MW: 287.994
Storage: 2-8 degree Celsius
SMILES: BrC1=C(C=CC(=C1C(F)(F)F)F)[N+](=O)[O-]
For R&D use only. Not for human or animal use.
CAS NO.: 1805937-67-0; 2-bromo-4-fluoro-1-nitro-3-(trifluoromethyl)benzene. PROPERTIES: This polyhalogenated aromatic compound features a bromine atom, a fluorine atom, a nitro group, and a trifluoromethyl group on a benzene ring, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The 2-bromo-4-fluoro-1-nitro-3-(trifluoromethyl)benzene typically appears as a white to off-white crystalline solid with moderate 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 2-bromo-4-fluoro-1-nitro-3-(trifluoromethyl)benzene serves as a valuable intermediate in the synthesis of highly functionalized aromatic compounds and materials with specific electronic properties. The nitro group provides a handle for further functionalization through reduction to amine or other transformations. In medicinal chemistry, this compound functions as a building block for developing pharmaceuticals targeting enzyme inhibitors and receptor modulators. The multiple halogen substituents contribute to target binding affinity and selectivity. 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 substitution pattern, enabling the development of advanced materials with tailored electronic characteristics.
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