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Atomfair Methyl4,6-dichloronicotinate C7H5Cl2NO2

Description Methyl 4,6-Dichloronicotinate (CAS No. 65973-52-6) is a high-purity chemical compound with the molecular formula C7H5Cl2NO2, widely utilized in pharmaceutical and agrochemical research. This fine chemical, also known as methyl 4,6-dichloropyridine-3-carboxylate, is a versatile intermediate for synthesizing active ingredients and specialty materials. Its dichlorinated pyridine structure offers excellent reactivity for nucleophilic substitution and cross-coupling reactions. Available in >98% purity (HPLC), it is supplied in rigorously tested batches with detailed Certificates of Analysis (CoA) to ensure consistency for sensitive applications. Suitable for use in medicinal chemistry, crop protection R&D, and as a building block for heterocyclic compounds.

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Description

Description

Methyl 4,6-Dichloronicotinate (CAS No. 65973-52-6) is a high-purity chemical compound with the molecular formula C7H5Cl2NO2, widely utilized in pharmaceutical and agrochemical research. This fine chemical, also known as methyl 4,6-dichloropyridine-3-carboxylate, is a versatile intermediate for synthesizing active ingredients and specialty materials. Its dichlorinated pyridine structure offers excellent reactivity for nucleophilic substitution and cross-coupling reactions. Available in >98% purity (HPLC), it is supplied in rigorously tested batches with detailed Certificates of Analysis (CoA) to ensure consistency for sensitive applications. Suitable for use in medicinal chemistry, crop protection R&D, and as a building block for heterocyclic compounds.

  • CAS No: 65973-52-6
  • Molecular Formula: C7H5Cl2NO2
  • Molecular Weight: 206.02
  • Exact Mass: 204.9697338
  • Monoisotopic Mass: 204.9697338
  • IUPAC Name: methyl 4,6-dichloropyridine-3-carboxylate
  • SMILES: COC(=O)C1=CN=C(C=C1Cl)Cl
  • Synonyms: Methyl4,6-dichloronicotinate, 689-863-8, methyl 4,6-dichloronicotinate, 65973-52-6, methyl 4,6-dichloropyridine-3-carboxylate

Application

Methyl 4,6-Dichloronicotinate serves as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and antibacterial agents. Its reactive dichloro groups enable efficient functionalization for creating complex pyridine derivatives used in crop protection chemicals. Researchers also employ this compound in metal-catalyzed cross-coupling reactions to construct biologically active molecules.

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