Description
Ethyl 4-hydroxy-3-iodobenzoate (CAS No. 15126-07-5) is a high-purity iodinated benzoate ester with the molecular formula C9H9IO3. This compound is a valuable synthetic intermediate for pharmaceutical, agrochemical, and materials science research. Its unique structure, featuring both a hydroxyl group and an iodine substituent on the aromatic ring, makes it a versatile building block for further functionalization. Available in >98% purity (HPLC), this product is rigorously tested for consistency and stability, ensuring reliable performance in demanding applications. Packaged under inert gas to prevent degradation, it is supplied in amber glass vials with certificates of analysis.
Properties
- CAS Number: 15126-07-5
- Complexity: 184
- IUPAC Name: ethyl 4-hydroxy-3-iodo-benzoate
- InChI: InChI=1S/C9H9IO3/c1-2-13-9(12)6-3-4-8(11)7(10)5-6/h3-5,11H,2H2,1H3
- InChI Key: HOAXKZYYZXASLJ-UHFFFAOYSA-N
- Exact Mass: 291.95964
- Molecular Formula: C9H9IO3
- Molecular Weight: 292.07
- SMILES: CCOC(=O)C1=CC(=C(C=C1)O)I
- Topological: 46.5
- Monoisotopic Mass: 291.95964
- Synonyms: Ethyl 4-hydroxy-3-iodobenzoate, 15126-07-5, Benzoic acid, 4-hydroxy-3-iodo-, ethyl ester, Ethyl4-hydroxy-3-iodobenzoate, Ethyl 4-hydroxy-3-iodo-benzoate, 4-Hydroxy-3-iodo-benzoic Acid Ethyl Ester, ETHYL-3-IODO-4-HYDROXY BENZOATE, MFCD11112908, SCHEMBL337806, DTXSID90459205, HOAXKZYYZXASLJ-UHFFFAOYSA-N, AKOS015843516, AS-30045, DB-063893, CS-0334024
Application
Ethyl 4-hydroxy-3-iodobenzoate serves as a key intermediate in Suzuki-Miyaura cross-coupling reactions for synthesizing biaryl compounds. Researchers utilize its iodine moiety for palladium-catalyzed transformations in drug discovery programs targeting kinase inhibitors. The compound’s hydroxyl group also enables facile derivatization for polymer-bound catalysts or fluorescent probes in material science applications.
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