2,6-dichloro-4-iodophenol
$300.00
CAS No.: 34074-22-1
Catalog No.: WLZ1614
Purity: 95%
MF: C6H3Cl2IO
MW: 288.899
Storage: 2-8 degree Celsius
SMILES: ClC1=C(C(=CC(=C1)I)Cl)O
Catalog No.: WLZ1614
Purity: 95%
MF: C6H3Cl2IO
MW: 288.899
Storage: 2-8 degree Celsius
SMILES: ClC1=C(C(=CC(=C1)I)Cl)O
CAS NO.: 34074-22-1; 2,6-dichloro-4-iodophenol. PROPERTIES: This halogenated aromatic compound features two chlorine atoms and an iodine atom on a phenol ring, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The 2,6-dichloro-4-iodophenol typically appears as a white crystalline powder with limited aqueous solubility but good solubility in common organic solvents. Its molecular structure includes multiple halogen atoms and a hydroxy group 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 2,6-dichloro-4-iodophenol serves as a valuable intermediate in the synthesis of highly functionalized aromatic compounds and materials with specific electronic properties. The iodine substituent provides a handle for cross-coupling reactions, enabling the creation of substituted benzene derivatives with diverse biological activities. In medicinal chemistry, this compound functions as a building block for developing pharmaceuticals targeting enzyme inhibitors and receptor modulators. The hydroxy group can be further modified for additional diversification. 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 functional group versatility, enabling the development of diverse molecular architectures for applications ranging from drug discovery to advanced materials.
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