Atomfair 6-Chloro-2-methyl-3-nitropyridine C6H5ClN2O2

Description 6-Chloro-2-methyl-3-nitropyridine (CAS No. 22280-60-0) is a high-purity nitropyridine derivative with the molecular formula C6H5ClN2O2, widely utilized in pharmaceutical and agrochemical research. This compound features a chloro-substituted pyridine ring with methyl and nitro functional groups at the 2- and 3-positions, respectively, making it a versatile intermediate for heterocyclic synthesis. With a molecular weight of 172.57 g/mol, it is supplied as a crystalline solid with ??98% purity (HPLC) and is rigorously tested for consistency. Ideal for nucleophilic substitution reactions, cross-coupling methodologies, and as a precursor for bioactive molecules. Packaged under inert gas to ensure stability and shipped with detailed analytical certificates…

Description

Description

6-Chloro-2-methyl-3-nitropyridine (CAS No. 22280-60-0) is a high-purity nitropyridine derivative with the molecular formula C6H5ClN2O2, widely utilized in pharmaceutical and agrochemical research. This compound features a chloro-substituted pyridine ring with methyl and nitro functional groups at the 2- and 3-positions, respectively, making it a versatile intermediate for heterocyclic synthesis. With a molecular weight of 172.57 g/mol, it is supplied as a crystalline solid with ??98% purity (HPLC) and is rigorously tested for consistency. Ideal for nucleophilic substitution reactions, cross-coupling methodologies, and as a precursor for bioactive molecules. Packaged under inert gas to ensure stability and shipped with detailed analytical certificates (GC/MS, NMR).

  • CAS No: 22280-60-0
  • Molecular Formula: C6H5ClN2O2
  • Molecular Weight: 172.57
  • Exact Mass: 172.0039551
  • Monoisotopic Mass: 172.0039551
  • IUPAC Name: 6-chloro-2-methyl-3-nitropyridine
  • SMILES: CC1=C(C=CC(=N1)Cl)[N+](=O)[O-]
  • Synonyms: 6-Chloro-2-methyl-3-nitropyridine, 22280-60-0, DTXSID50291446, DTXCID10242590, 640-315-6

Application

6-Chloro-2-methyl-3-nitropyridine serves as a key building block in the synthesis of pharmaceuticals, particularly for antimalarial and antiviral agents. Its nitro group facilitates reduction to amines for further functionalization, while the chloro substituent enables palladium-catalyzed cross-coupling reactions. Researchers also employ it in agrochemical development for crop protection compounds. The compound’s reactivity is leveraged in material science for creating nitrogen-containing heterocycles.

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