4-hydroxy-2-(trifluoromethyl)benzonitrile

4-hydroxy-2-(trifluoromethyl)benzonitrile

4-iodo-3-(trifluoromethyl)benzonitrile

4-iodo-3-(trifluoromethyl)benzonitrile

4-iodo-2-methoxybenzaldehyde

$488.00
CAS No.: 139102-37-7
Catalog No.: WLZ1764
Purity: 95%
MF: C8H7IO2
MW: 262.046
Storage: 2-8 degree Celsius
SMILES: IC1=CC(=C(C=O)C=C1)OC
For R&D use only. Not for human or animal use.
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CAS NO.: 139102-37-7; 4-iodo-2-methoxybenzaldehyde. PROPERTIES: This iodinated aromatic aldehyde features an iodine atom and a methoxy group on a benzene ring connected to an aldehyde group, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The 4-iodo-2-methoxybenzaldehyde typically appears as a white to off-white crystalline solid with moderate solubility in common organic solvents. Its molecular structure includes an electron-donating methoxy group and an electron-withdrawing iodine 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 4-iodo-2-methoxybenzaldehyde serves as a valuable intermediate in the synthesis of highly functionalized aromatic compounds and materials with specific electronic properties. The aldehyde group provides a handle for further functionalization through reactions such as reduction or oxidation. In medicinal chemistry, this compound functions as a building block for developing pharmaceuticals targeting enzyme inhibitors and receptor modulators. The iodine substituent contributes 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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