methyl 3,5-dichloro-2-methoxybenzoate
$200.00
CAS No.: 64122-23-2
Catalog No.: WLZ1799
Purity: 95%
MF: C9H8Cl2O3
MW: 235.066
Storage: 2-8 degree Celsius
SMILES: ClC=1C(=C(C(=O)OC)C=C(C1)Cl)OC
Catalog No.: WLZ1799
Purity: 95%
MF: C9H8Cl2O3
MW: 235.066
Storage: 2-8 degree Celsius
SMILES: ClC=1C(=C(C(=O)OC)C=C(C1)Cl)OC
CAS NO.: 64122-23-2; methyl 3,5-dichloro-2-methoxybenzoate. PROPERTIES: This highly chlorinated aromatic ester features two chlorine atoms and a methoxy group on a benzene ring connected to a methyl ester group, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The methyl 3,5-dichloro-2-methoxybenzoate typically appears as a white crystalline powder with moderate aqueous solubility. Its molecular structure includes electron-donating methoxy and electron-withdrawing chlorine atoms 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 methyl 3,5-dichloro-2-methoxybenzoate serves as a valuable intermediate in the synthesis of pharmaceuticals, particularly those targeting enzyme inhibitors and receptor modulators. 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 antiviral and anticancer agents where the methoxy and chlorine groups contribute 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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