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Atomfair Methyl 3-chloro-5-iodobenzoate C8H6ClIO2

Description Methyl 3-chloro-5-iodobenzoate (CAS No. 1261559-47-0) is a high-purity halogenated benzoate ester with the molecular formula C8H6ClIO2. This compound is a versatile intermediate in organic synthesis, particularly in pharmaceutical and agrochemical research. Its unique structure, featuring both chloro and iodo substituents on the aromatic ring, makes it a valuable building block for cross-coupling reactions, such as Suzuki-Miyaura and Stille couplings. The methyl ester group enhances solubility in organic solvents, facilitating further derivatization. Supplied as a crystalline solid with ??95% purity (HPLC), it is rigorously tested for consistency and stability. Ideal for researchers developing novel bioactive molecules or materials science applications.

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Description

Description

Methyl 3-chloro-5-iodobenzoate (CAS No. 1261559-47-0) is a high-purity halogenated benzoate ester with the molecular formula C8H6ClIO2. This compound is a versatile intermediate in organic synthesis, particularly in pharmaceutical and agrochemical research. Its unique structure, featuring both chloro and iodo substituents on the aromatic ring, makes it a valuable building block for cross-coupling reactions, such as Suzuki-Miyaura and Stille couplings. The methyl ester group enhances solubility in organic solvents, facilitating further derivatization. Supplied as a crystalline solid with ??95% purity (HPLC), it is rigorously tested for consistency and stability. Ideal for researchers developing novel bioactive molecules or materials science applications.

  • CAS No: 1261559-47-0
  • Molecular Formula: C8H6ClIO2
  • Molecular Weight: 296.49
  • Exact Mass: 295.91010
  • Monoisotopic Mass: 295.91010
  • IUPAC Name: methyl 3-chloro-5-iodobenzoate
  • SMILES: COC(=O)C1=CC(=CC(=C1)I)Cl
  • Synonyms: Methyl 3-chloro-5-iodobenzoate, 289039-85-6, Benzoic acid, 3-chloro-5-iodo-, methyl ester, DTXSID90641027, DTXCID70591778

Application

Methyl 3-chloro-5-iodobenzoate is widely used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its halogenated aromatic core enables efficient participation in palladium-catalyzed cross-coupling reactions to construct complex biaryl structures. Researchers utilize this compound in the development of kinase inhibitors and other small-molecule therapeutics. It also serves as a precursor for liquid crystal materials and advanced polymers.

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