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Atomfair 3-Chloro-2-iodopyridine C5H3ClIN

Description 3-Chloro-2-iodopyridine (CAS No. 77332-89-9) is a high-purity halogenated pyridine derivative with the molecular formula C5H3ClIN , widely utilized in pharmaceutical and agrochemical research. This compound serves as a versatile building block for cross-coupling reactions (e.g., Suzuki, Stille, Negishi) due to its reactive iodine and chlorine substituents, enabling precise functionalization of the pyridine ring. Provided as a crystalline solid with ??95% purity (HPLC), it is rigorously tested for consistency in batch-to-batch performance. Ideal for synthesizing ligands, catalysts, and bioactive molecules, it is packaged under inert conditions to ensure stability. Available in quantities from grams to kilograms, with optional custom purity…

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Description

Description

3-Chloro-2-iodopyridine (CAS No. 77332-89-9) is a high-purity halogenated pyridine derivative with the molecular formula C5H3ClIN, widely utilized in pharmaceutical and agrochemical research. This compound serves as a versatile building block for cross-coupling reactions (e.g., Suzuki, Stille, Negishi) due to its reactive iodine and chlorine substituents, enabling precise functionalization of the pyridine ring. Provided as a crystalline solid with ??95% purity (HPLC), it is rigorously tested for consistency in batch-to-batch performance. Ideal for synthesizing ligands, catalysts, and bioactive molecules, it is packaged under inert conditions to ensure stability. Available in quantities from grams to kilograms, with optional custom purity and packaging.

  • CAS No: 77332-89-9
  • Molecular Formula: C5H3ClIN
  • Molecular Weight: 239.44
  • Exact Mass: 238.89987
  • Monoisotopic Mass: 238.89987
  • IUPAC Name: 3-chloro-2-iodopyridine
  • SMILES: C1=CC(=C(N=C1)I)Cl
  • Synonyms: 3-chloro-2-iodopyridine, 77332-89-9, DTXSID00445770, DTXCID00396591, 811-259-1

Application

3-Chloro-2-iodopyridine is a key intermediate in pharmaceutical synthesis, particularly for designing kinase inhibitors and antiviral agents. Its halogenated structure facilitates palladium-catalyzed couplings to construct complex heterocycles. Researchers also employ it in material science to develop functionalized ligands for metal-organic frameworks (MOFs).

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