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Atomfair 6-Chloropyridin-2-ol C5H4ClNO

Description 6-Chloropyridin-2-ol (CAS No. 41288-96-4) is a high-purity heterocyclic organic compound with the molecular formula C5H4ClNO . Also known as 6-chloro-1H-pyridin-2-one , this versatile chemical building block features a chlorinated pyridine ring with a hydroxyl group at the 2-position, offering unique reactivity for nucleophilic substitutions and metal-catalyzed cross-coupling reactions. Our product is synthesized under strict quality control, delivering ??98% purity (HPLC) with low trace metal content, ideal for pharmaceutical intermediates, agrochemical research, and ligand synthesis. Available in crystalline powder form with batch-specific COA, NMR, and MSDS documentation. Store in a cool, dry place under inert atmosphere for optimal stability.

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Description

Description

6-Chloropyridin-2-ol (CAS No. 41288-96-4) is a high-purity heterocyclic organic compound with the molecular formula C5H4ClNO. Also known as 6-chloro-1H-pyridin-2-one, this versatile chemical building block features a chlorinated pyridine ring with a hydroxyl group at the 2-position, offering unique reactivity for nucleophilic substitutions and metal-catalyzed cross-coupling reactions. Our product is synthesized under strict quality control, delivering ??98% purity (HPLC) with low trace metal content, ideal for pharmaceutical intermediates, agrochemical research, and ligand synthesis. Available in crystalline powder form with batch-specific COA, NMR, and MSDS documentation. Store in a cool, dry place under inert atmosphere for optimal stability.

  • CAS No: 41288-96-4
  • Molecular Formula: C5H4ClNO
  • Molecular Weight: 129.54
  • Exact Mass: 128.9981414
  • Monoisotopic Mass: 128.9981414
  • IUPAC Name: 6-chloro-1H-pyridin-2-one
  • SMILES: C1=CC(=O)NC(=C1)Cl
  • Synonyms: 6-Chloropyridin-2-ol, 2(1H)-Pyridinone, 6-chloro-, 6-Chloro-2(1H)-pyridinone, EINECS 240-909-1, NSC 148331

Application

6-Chloropyridin-2-ol serves as a key intermediate in the synthesis of antiviral and antibacterial agents, particularly in quinolone antibiotic derivatives. Its reactive chloro and hydroxyl groups enable facile functionalization for constructing complex heterocycles in medicinal chemistry. Researchers also utilize this compound as a precursor for N-alkylated pyridone ligands in transition metal catalysis.

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