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Atomfair 4-Iodo-N-methoxy-N-methyl-benzamide C9H10INO2

Description 4-Iodo-N-methoxy-N-methylbenzamide (CAS No. 187617-01-2) is a high-purity organic compound with the molecular formula C9H10INO2. This benzamide derivative features an iodine substituent at the para position, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. The compound’s unique structure, incorporating both methoxy and N-methyl functional groups, enhances its reactivity in cross-coupling reactions and other transformations. It is supplied as a crystalline solid with ??95% purity (HPLC), ensuring consistency for research applications. Ideal for use in Suzuki-Miyaura couplings, amidation reactions, and as a precursor for bioactive molecule synthesis.

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Description

Description

4-Iodo-N-methoxy-N-methylbenzamide (CAS No. 187617-01-2) is a high-purity organic compound with the molecular formula C9H10INO2. This benzamide derivative features an iodine substituent at the para position, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. The compound’s unique structure, incorporating both methoxy and N-methyl functional groups, enhances its reactivity in cross-coupling reactions and other transformations. It is supplied as a crystalline solid with ??95% purity (HPLC), ensuring consistency for research applications. Ideal for use in Suzuki-Miyaura couplings, amidation reactions, and as a precursor for bioactive molecule synthesis.

  • CAS No: 187617-01-2
  • Molecular Formula: C9H10INO2
  • Molecular Weight: 291.09
  • Exact Mass: 290.97563
  • Monoisotopic Mass: 290.97563
  • IUPAC Name: 4-iodo-N-methoxy-N-methylbenzamide
  • SMILES: CN(C(=O)C1=CC=C(C=C1)I)OC
  • Synonyms: 187617-01-2, 4-Iodo-N-methoxy-N-methyl-benzamide, DTXSID90420137, DTXCID70370984, 4-iodo-N-methoxy-N-methylbenzamide

Application

4-Iodo-N-methoxy-N-methylbenzamide serves as a versatile building block in medicinal chemistry, particularly for the synthesis of kinase inhibitors and other pharmacologically active compounds. Its iodine moiety facilitates palladium-catalyzed cross-coupling reactions, enabling rapid diversification of molecular scaffolds. Researchers utilize this compound in the development of PET radiotracers due to the radioactive isotope compatibility of its aromatic iodine. It also finds application in materials science as a precursor for liquid crystals and organic electronic materials.

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