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Atomfair Ethyl 4-hydroxy-3-iodobenzoate C9H9IO3

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.

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Description

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.

  • CAS No: 15126-07-5
  • Molecular Formula: C9H9IO3
  • Molecular Weight: 292.07
  • Exact Mass: 291.95964
  • Monoisotopic Mass: 291.95964
  • IUPAC Name: ethyl 4-hydroxy-3-iodobenzoate
  • SMILES: CCOC(=O)C1=CC(=C(C=C1)O)I
  • 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

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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