2,3-difluoro-6-methoxyaniline
$300.00
CAS No.: 886501-51-5
Catalog No.: WLZ1593
Purity: 95%
MF: C7H7F2NO
MW: 159.135
Storage: 2-8 degree Celsius
SMILES: FC1=C(N)C(=CC=C1F)OC
Catalog No.: WLZ1593
Purity: 95%
MF: C7H7F2NO
MW: 159.135
Storage: 2-8 degree Celsius
SMILES: FC1=C(N)C(=CC=C1F)OC
CAS NO.: 886501-51-5; 2,3-difluoro-6-methoxyaniline. PROPERTIES: This aromatic amine features fluorine substituents and a methoxy group on a benzene ring, creating a molecule with potential applications in medicinal chemistry and pharmaceutical research. The 2,3-difluoro-6-methoxyaniline typically appears as a white crystalline powder with moderate aqueous solubility. Its molecular structure includes electron-withdrawing fluorine atoms and an electron-donating methoxy group that influence the electronic properties of the aromatic system. For optimal stability, this compound should be stored at 2-8 degree Celsius in a tightly sealed container away from moisture and direct light. When handling, chemists should wear appropriate personal protective equipment including nitrile gloves and safety goggles. This compound is hygroscopic and may form salts upon exposure to atmospheric moisture. In case of accidental ingestion, rinse mouth thoroughly and seek medical attention. APPLICATIONS: The 2,3-difluoro-6-methoxyaniline serves as a valuable intermediate in the synthesis of pharmaceuticals, particularly those targeting enzyme inhibitors and receptor modulators. The fluorine substituents provide a bioisosteric replacement that can enhance metabolic stability and target binding affinity. In medicinal chemistry, this compound functions as a building block for developing antiviral and anticancer agents where the aromatic amine functionality contributes to target engagement. Additionally, the molecule finds utility in chemical biology studies where its unique scaffold can be used to probe enzyme inhibition mechanisms and cellular signaling pathways. Researchers utilizing this compound benefit from its defined electronic properties and functional group arrangement, advancing investigations into novel therapeutic approaches for various disease conditions.
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