methyl 5-amino-2-fluoro-4-methoxybenzoate
$350.00
CAS No.: 1785259-87-1
Catalog No.: WLZ1819
Purity: 95%
MF: C9H10FNO3
MW: 199.181
Storage: 2-8 degree Celsius
SMILES: NC=1C(=CC(=C(C(=O)OC)C1)F)OC
Catalog No.: WLZ1819
Purity: 95%
MF: C9H10FNO3
MW: 199.181
Storage: 2-8 degree Celsius
SMILES: NC=1C(=CC(=C(C(=O)OC)C1)F)OC
CAS NO.: 1785259-87-1; methyl 5-amino-2-fluoro-4-methoxybenzoate. PROPERTIES: This fluoromethoxybenzoate features an amine group and a fluorine atom on a benzene ring connected to a methyl ester group, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The methyl 5-amino-2-fluoro-4-methoxybenzoate typically appears as a white to off-white crystalline solid with moderate solubility in common organic solvents. Its molecular structure includes electron-donating methoxy and amine groups and an electron-withdrawing fluorine atom 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 methyl 5-amino-2-fluoro-4-methoxybenzoate serves as a valuable intermediate in the synthesis of highly functionalized aromatic compounds and materials with specific electronic properties. The ester group provides a handle for further functionalization through hydrolysis to the corresponding carboxylic acid or transesterification. In medicinal chemistry, this compound functions as a building block for developing pharmaceuticals targeting enzyme inhibitors and receptor modulators. The fluorine and methoxy 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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