1,3-dinitro-4,6-difluorobenzene
$325.00
CAS No.: 327-92-4
Catalog No.: WLZ1572
Purity: 95%
MF: C6H2F2N2O4
MW: 204.088
Storage: 2-8 degree Celsius
SMILES: [N+](=O)([O-])C1=CC(=C(C=C1F)F)[N+](=O)[O-]
Catalog No.: WLZ1572
Purity: 95%
MF: C6H2F2N2O4
MW: 204.088
Storage: 2-8 degree Celsius
SMILES: [N+](=O)([O-])C1=CC(=C(C=C1F)F)[N+](=O)[O-]
CAS NO.: 327-92-4; 1,3-dinitro-4,6-difluorobenzene. PROPERTIES: This nitrofluorinated aromatic compound features two nitro groups and two fluorine atoms on a benzene ring, creating a molecule with potential applications in organic synthesis and explosives research. The 1,3-dinitro-4,6-difluorobenzene typically appears as a white crystalline powder with limited aqueous solubility but good solubility in common organic solvents. Its molecular structure includes electron-withdrawing nitro groups and fluorine atoms that influence the electronic properties of the aromatic system. For optimal stability and to prevent premature reactions, 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-dinitro-4,6-difluorobenzene serves as a valuable intermediate in the synthesis of highly energetic materials and explosives. The nitro groups provide high energy density and oxidative potential. In organic synthesis, this compound functions as a building block for creating fluoroacyl-containing bioactive molecules. The fluorine atoms contribute to target binding affinity and selectivity in medicinal chemistry applications. 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 functional group versatility, enabling the development of diverse molecular architectures for applications ranging from energetic materials to advanced materials.
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