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Atomfair 4-Iodo-3-nitrobenzoic acid C7H4INO4

Description 4-Iodo-3-nitrobenzoic acid (CAS No. 35674-27-2) is a high-purity aromatic carboxylic acid derivative with the molecular formula C7H4INO4. This compound features both an iodine substituent and a nitro group ortho to the carboxylic acid functionality, making it a versatile intermediate in organic synthesis and pharmaceutical research. Its crystalline solid form and well-defined structure (IUPAC name: 4-iodo-3-nitrobenzoic acid ) ensure consistent reactivity in coupling reactions, halogen exchange processes, and as a precursor for heterocyclic compounds. Ideal for researchers requiring precise electrophilic aromatic substitution or metal-catalyzed cross-coupling reactions. Packaged under inert conditions to guarantee stability and purity (>95% by HPLC).

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Description

Description

4-Iodo-3-nitrobenzoic acid (CAS No. 35674-27-2) is a high-purity aromatic carboxylic acid derivative with the molecular formula C7H4INO4. This compound features both an iodine substituent and a nitro group ortho to the carboxylic acid functionality, making it a versatile intermediate in organic synthesis and pharmaceutical research. Its crystalline solid form and well-defined structure (IUPAC name: 4-iodo-3-nitrobenzoic acid) ensure consistent reactivity in coupling reactions, halogen exchange processes, and as a precursor for heterocyclic compounds. Ideal for researchers requiring precise electrophilic aromatic substitution or metal-catalyzed cross-coupling reactions. Packaged under inert conditions to guarantee stability and purity (>95% by HPLC).

  • CAS No: 35674-27-2
  • Molecular Formula: C7H4INO4
  • Molecular Weight: 293.02
  • Exact Mass: 292.91851
  • Monoisotopic Mass: 292.91851
  • IUPAC Name: 4-iodo-3-nitrobenzoic acid
  • SMILES: C1=CC(=C(C=C1C(=O)O)[N+](=O)[O-])I
  • Synonyms: 4-iodo-3-nitrobenzoic acid, 35674-27-2, DTXSID70458857, DTXCID60409676, 670-347-6

Application

4-Iodo-3-nitrobenzoic acid serves as a key building block in medicinal chemistry for the synthesis of nitroaromatic pharmacophores. It is utilized in Suzuki-Miyaura cross-coupling reactions to create biaryl structures for drug discovery. The compound also finds application in materials science as a precursor for iodine-containing polymers and liquid crystals. Its reactive iodine and nitro groups enable facile derivatization in agrochemical research.

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