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Atomfair Ethyl 4,5-dichloro-1H-pyrazole-3-carboxylate C6H6Cl2N2O2

Description Ethyl 4,5-dichloro-1H-pyrazole-3-carboxylate (CAS No. 1872370-57-4) is a high-purity pyrazole derivative with the molecular formula C6H6Cl2N2O2. This compound is a versatile building block in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and specialty materials. Its reactive dichloro and ester functional groups make it an ideal intermediate for further functionalization. The product is supplied as a crystalline solid with >95% purity (HPLC), ensuring consistency for research and industrial applications. Proper storage under inert conditions is recommended to maintain stability.

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Description

Description

Ethyl 4,5-dichloro-1H-pyrazole-3-carboxylate (CAS No. 1872370-57-4) is a high-purity pyrazole derivative with the molecular formula C6H6Cl2N2O2. This compound is a versatile building block in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and specialty materials. Its reactive dichloro and ester functional groups make it an ideal intermediate for further functionalization. The product is supplied as a crystalline solid with >95% purity (HPLC), ensuring consistency for research and industrial applications. Proper storage under inert conditions is recommended to maintain stability.

  • CAS No: 1872370-57-4
  • Molecular Formula: C6H6Cl2N2O2
  • Molecular Weight: 209.03
  • Exact Mass: 207.9806328
  • Monoisotopic Mass: 207.9806328
  • IUPAC Name: ethyl 4,5-dichloro-1H-pyrazole-3-carboxylate
  • SMILES: CCOC(=O)C1=NNC(=C1Cl)Cl
  • Synonyms: Ethyl 4,5-dichloro-1H-pyrazole-3-carboxylate

Application

Ethyl 4,5-dichloro-1H-pyrazole-3-carboxylate serves as a key intermediate in medicinal chemistry for the synthesis of bioactive pyrazole scaffolds. It is utilized in the development of potential antiviral and anticancer agents due to its reactive halogen substituents. The compound also finds use in agrochemical research for creating novel pesticides and herbicides. Its ester group allows for further derivatization via hydrolysis or nucleophilic substitution reactions.

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