6-bromo-2-fluoro-3-(trifluoromethoxy)benzaldehyde
$300.00
CAS No.: 524674-70-2
Catalog No.: WLZ1636
Purity: 95%
MF: C8H3BrF4O2
MW: 287.006
Storage: 2-8 degree Celsius
SMILES: O=CC1=C(Br)C=CC(OC(F)(F)F)=C1F
Catalog No.: WLZ1636
Purity: 95%
MF: C8H3BrF4O2
MW: 287.006
Storage: 2-8 degree Celsius
SMILES: O=CC1=C(Br)C=CC(OC(F)(F)F)=C1F
CAS NO.: 524674-70-2; 6-bromo-2-fluoro-3-(trifluoromethoxy)benzaldehyde. PROPERTIES: This halogenated aromatic aldehyde features a bromine atom, a fluorine atom, and a trifluoromethoxy group on a benzene ring connected to an aldehyde group, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The 6-bromo-2-fluoro-3-(trifluoromethoxy)benzaldehyde typically appears as a white to off-white crystalline solid with moderate solubility in common organic solvents. Its molecular structure includes electron-withdrawing trifluoromethoxy and fluorine groups 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 6-bromo-2-fluoro-3-(trifluoromethoxy)benzaldehyde serves as a valuable intermediate in the synthesis of highly functionalized aromatic compounds and materials with specific electronic properties. The bromine substituent provides a handle 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 trifluoromethoxy and fluorine 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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