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CS-W001157 4
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6-Chloro-5-nitro-2-picoline

  • CAS No. 56057-19-3

  • Cat. No. CS-0007518
  • Purity≥98%
  • MDL No.MFCD03085820

*For research and further manufacturing use only, not for direct human use.

6-Chloro-5-nitro-2-picoline|CS-0007518

Structure of 56057-19-3

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General Information

  • CAS No. 56057-19-3
  • Cat. No. CS-0007518
  • Purity ≥98%
  • MDL No. MFCD03085820
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₅ClN₂O₂
  • Molecular Weight 172.57
  • Synonym(s) 2-Chloro-6-methyl-3-nitropyridine; 6-Chloro-5-nitro-2-picoline
  • SMILES O=[N+](C1=CC=C(C)N=C1Cl)[O-]

Description

6-Chloro-5-nitro-2-picoline features a chlorinated pyridine core with complementary nitro and methyl substituents, enabling direct incorporation into heterocyclic scaffolds. The electron-deficient aromatic ring facilitates nucleophilic substitution reactions under mild conditions, while the para-oriented nitro group enhances reactivity in cross-coupling processes. This bench-stable compound serves as a key intermediate for advanced pharmaceutical and agrochemical synthesis.

Application

6-Chloro-5-nitro-2-picoline serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the pyridine ring due to orthogonal reactivity of the chloro and nitro groups. The chloro substituent facilitates palladium-catalyzed cross-coupling reactions, while the nitro group supports subsequent reduction to an amino moiety, offering access to diverse heterocyclic scaffolds. Its bench-stable nature and compatibility with standard purification methods make it well-suited for multi-step synthesis workflows.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   56.03
  • LogP   1.95162
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   1

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