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Atomfair 2,3-Dichloro-5-nitropyridine C5H2Cl2N2O2

Description 2,3-Dichloro-5-nitropyridine (CAS No. 22353-40-8) is a high-purity heterocyclic compound with the molecular formula C5H2Cl2N2O2. This nitro-substituted pyridine derivative is a versatile building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its distinct structure, featuring two chlorine atoms and a nitro group on the pyridine ring, enables selective functionalization for the development of complex molecules. Available in >98% purity (HPLC), this compound is rigorously tested for consistency and stability. Suitable for use in cross-coupling reactions, nucleophilic substitutions, and as a precursor for bioactive compounds. Packaged under inert gas to ensure longevity and shipped with comprehensive analytical data (GC/MS,…

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Description

Description

2,3-Dichloro-5-nitropyridine (CAS No. 22353-40-8) is a high-purity heterocyclic compound with the molecular formula C5H2Cl2N2O2. This nitro-substituted pyridine derivative is a versatile building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its distinct structure, featuring two chlorine atoms and a nitro group on the pyridine ring, enables selective functionalization for the development of complex molecules. Available in >98% purity (HPLC), this compound is rigorously tested for consistency and stability. Suitable for use in cross-coupling reactions, nucleophilic substitutions, and as a precursor for bioactive compounds. Packaged under inert gas to ensure longevity and shipped with comprehensive analytical data (GC/MS, NMR).

  • CAS No: 22353-40-8
  • Molecular Formula: C5H2Cl2N2O2
  • Molecular Weight: 192.98
  • Exact Mass: 191.9493327
  • Monoisotopic Mass: 191.9493327
  • IUPAC Name: 2,3-dichloro-5-nitropyridine
  • SMILES: C1=C(C=NC(=C1Cl)Cl)[N+](=O)[O-]
  • Synonyms: 2,3-Dichloro-5-nitropyridine, 22353-40-8, Pyridine, 2,3-dichloro-5-nitro-, DTXSID90376741, DTXCID00327769

Application

2,3-Dichloro-5-nitropyridine serves as a key intermediate in the synthesis of pharmaceuticals, including potential kinase inhibitors and antimicrobial agents. Its reactive sites facilitate Suzuki-Miyaura and Buchwald-Hartwig couplings for drug discovery. In material science, it contributes to the development of liquid crystals and OLED precursors. The nitro group also allows reduction to amino derivatives for further functionalization.

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