Your cart is currently empty!

Atomfair 2-Fluoro-5-iodobenzoic acid C7H4FIO2
Description 2-Fluoro-5-iodobenzoic acid (CAS No. 124700-41-0) is a high-purity halogenated benzoic acid derivative with the molecular formula C7H4FIO2. This compound features a fluorine atom at the ortho position and an iodine substituent at the meta position relative to the carboxylic acid group, making it a versatile building block for pharmaceutical, agrochemical, and materials science research. With a molecular weight of 266.01 g/mol, it is supplied as a white to off-white crystalline powder with ??95% purity (HPLC). Ideal for Suzuki coupling, cross-coupling reactions, and as a precursor for radiolabeling studies due to the reactive iodine moiety. Store in a cool, dry…
Description
Description
2-Fluoro-5-iodobenzoic acid (CAS No. 124700-41-0) is a high-purity halogenated benzoic acid derivative with the molecular formula C7H4FIO2. This compound features a fluorine atom at the ortho position and an iodine substituent at the meta position relative to the carboxylic acid group, making it a versatile building block for pharmaceutical, agrochemical, and materials science research. With a molecular weight of 266.01 g/mol, it is supplied as a white to off-white crystalline powder with ??95% purity (HPLC). Ideal for Suzuki coupling, cross-coupling reactions, and as a precursor for radiolabeling studies due to the reactive iodine moiety. Store in a cool, dry place under inert conditions to ensure stability.
- CAS No: 124700-41-0
- Molecular Formula: C7H4FIO2
- Molecular Weight: 266.01
- Exact Mass: 265.92401
- Monoisotopic Mass: 265.92401
- IUPAC Name: 2-fluoro-5-iodobenzoic acid
- SMILES: C1=CC(=C(C=C1I)C(=O)O)F
- Synonyms: 2-Fluoro-5-iodobenzoic acid, 124700-41-0, DTXSID10381195, DTXCID30332220, 603-004-6
Application
2-Fluoro-5-iodobenzoic acid is widely used as a key intermediate in organic synthesis, particularly in the preparation of fluorinated and iodinated aromatic compounds for drug discovery. Its reactive iodine group enables efficient cross-coupling reactions (e.g., Sonogashira, Heck) to construct complex molecules. Researchers also utilize it in radiopharmaceutical development for PET imaging probes. The fluorine substituent enhances metabolic stability in bioactive molecules, making it valuable for medicinal chemistry applications.
If you are interested or have any questions, please contact us at support@atomfair.com