4-chloro-2-methoxy-N-methylaniline
$300.00
CAS No.: 35122-79-3
Catalog No.: WLZ1756
Purity: 95%
MF: C8H10ClNO
MW: 171.627
Storage: 2-8 degree Celsius
SMILES: ClC1=CC(=C(NC)C=C1)OC
Catalog No.: WLZ1756
Purity: 95%
MF: C8H10ClNO
MW: 171.627
Storage: 2-8 degree Celsius
SMILES: ClC1=CC(=C(NC)C=C1)OC
For R&D use only. Not for human or animal use.
CAS NO.: 35122-79-3; 4-chloro-2-methoxy-N-methylaniline. PROPERTIES: This methoxychlorinated aromatic amine features a chlorine atom and a methoxy group on a benzene ring connected to an N-methylamine group, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The 4-chloro-2-methoxy-N-methylaniline typically appears as a colorless to pale yellow liquid with moderate solubility in common organic solvents. Its molecular structure includes electron-donating methoxy and N-methyl groups and a chlorine atom 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 an amber glass bottle under an inert atmosphere. When handling, appropriate safety measures including nitrile gloves and safety goggles are recommended. This compound is sensitive to light and moisture, requiring careful environmental control during storage and use. In case of skin contact, wash thoroughly with soap and water; if eye contact occurs, rinse immediately and seek medical evaluation. APPLICATIONS: The 4-chloro-2-methoxy-N-methylaniline serves as a versatile building block in organic synthesis, particularly for creating methoxy-substituted bioactive molecules. The amine group provides a platform for developing pharmaceuticals targeting enzyme inhibitors and receptor modulators. In medicinal chemistry, this compound functions as an intermediate for creating antidepressant and anxiolytic agents where the substituted phenyl group 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 functional group versatility, enabling the development of diverse molecular architectures for applications ranging from drug discovery to advanced materials.
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