Description

N,N-Diethyl-3-hydroxy-4-iodobenzamide (CAS No. 911228-76-7) is a high-purity iodinated benzamide derivative with the molecular formula C₁₁H₁₄INO₂. This compound is a valuable synthetic intermediate for pharmaceutical and organic chemistry research, featuring a hydroxyl group and an iodine substituent on the benzene ring, which enhances its reactivity in cross-coupling reactions and other transformations. Its N,N-diethylamide moiety offers unique steric and electronic properties, making it useful in medicinal chemistry applications. Available in various quantities, this product is rigorously tested for purity and stability, ensuring reliable performance in your laboratory workflows. Store in a cool, dry place, protected from light to maintain optimal quality.

Properties

• CAS Number: 911228-76-7
• Complexity: 219
• IUPAC Name: N,N-diethyl-3-hydroxy-4-iodo-benzamide
• InChI: InChI=1S/C11H14INO2/c1-3-13(4-2)11(15)8-5-6-9(12)10(14)7-8/h5-7,14H,3-4H2,1-2H3
• InChI Key: TWESKHRGMRVGFR-UHFFFAOYSA-N
• Exact Mass: 319.00693
• Molecular Formula: C11H14INO2
• Molecular Weight: 319.14
• SMILES: CCN(CC)C(=O)C1=CC(=C(C=C1)I)O
• Topological: 40.5
• Monoisotopic Mass: 319.00693
• Synonyms: N,N-DIETHYL-3-HYDROXY-4-IODOBENZAMIDE, 911228-76-7, SCHEMBL471352, TWESKHRGMRVGFR-UHFFFAOYSA-N, A1-15816

Application

N,N-Diethyl-3-hydroxy-4-iodobenzamide is primarily employed as a key intermediate in the synthesis of bioactive molecules and pharmaceutical compounds. Its iodine substituent makes it a versatile substrate for palladium-catalyzed cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. Researchers also utilize this compound in the development of radiopharmaceuticals and imaging agents due to its iodinated structure. Additionally, it serves as a precursor in the synthesis of ligands for receptor-binding studies.

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