2-iodo-5-(trifluoromethyl)benzoic acid
$300.00
CAS No.: 702641-04-1
Catalog No.: WLZ1662
Purity: 95%
MF: C8H4F3IO2
MW: 316.016
Storage: 2-8 degree Celsius
SMILES: IC1=C(C(=O)O)C=C(C=C1)C(F)(F)F
Catalog No.: WLZ1662
Purity: 95%
MF: C8H4F3IO2
MW: 316.016
Storage: 2-8 degree Celsius
SMILES: IC1=C(C(=O)O)C=C(C=C1)C(F)(F)F
CAS NO.: 702641-04-1; 2-iodo-5-(trifluoromethyl)benzoic acid. PROPERTIES: This halogenated aromatic carboxylic acid features an iodine atom and a trifluoromethyl group on a benzene ring connected to a carboxylic acid group, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The 2-iodo-5-(trifluoromethyl)benzoic acid typically appears as a white crystalline powder with moderate aqueous solubility. Its molecular structure includes electron-withdrawing trifluoromethyl and iodine groups 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 2-iodo-5-(trifluoromethyl)benzoic acid serves as a valuable intermediate in the synthesis of pharmaceuticals, particularly those targeting enzyme inhibitors and receptor modulators. The iodine substituent provides a bioisosteric replacement that can enhance metabolic stability and target binding affinity. In medicinal chemistry, this compound functions as a building block for developing antiviral and anticancer agents where the carboxylic acid functionality 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 defined electronic properties and functional group arrangement, advancing investigations into novel therapeutic approaches for various disease conditions.
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