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CS-W001157 4
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Methyl 4-chloro-6-methoxypicolinate

  • CAS No. 204378-37-0

  • Cat. No. CS-0187504
  • Purity≥95%
  • MDL No.None

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

Methyl 4-chloro-6-methoxypicolinate|CS-0187504

Structure of 204378-37-0

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General Information

  • CAS No. 204378-37-0
  • Cat. No. CS-0187504
  • Purity ≥95%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₈ClNO₃
  • Molecular Weight 201.61
  • Synonym(s) 4-chloro-6-methoxypicolinic acid methyl ester
  • SMILES COC1=CC(=CC(=N1)C(=O)OC)Cl

Description

Methyl 4-chloro-6-methoxypicolinate features a pyridine core with orthogonal electron-withdrawing chlorine and electron-donating methoxy groups, enabling precise tuning of reactivity. This bench-stable ester integrates readily into synthetic sequences requiring regioselective functionalization or serves as a key intermediate in bioactive compound development.

Application

Methyl 4-chloro-6-methoxypicolinate serves as a versatile building block in medicinal chemistry, enabling efficient construction of substituted pyridine scaffolds. The chloro group facilitates nucleophilic substitution reactions, while the methyl ester supports selective reduction or functionalization. Its bench-stable nature and compatibility with standard coupling protocols make it well-suited for modular synthesis workflows targeting bioactive heterocycles.

Synthesis

  • Route1

    References

    • HEIMANN, Annekatrin; DAHMANN, Georg; GRUNDL, Marc; MUELLER, Stephan Georg; WELLENZOHN, Bernd Patent: US2013/158042 A1, 2013 ;
  • Route2

    References

    • HEIMANN, Annekatrin; DAHMANN, Georg; GRUNDL, Marc; MUELLER, Stephan Georg; WELLENZOHN, Bernd Patent: US2013/158042 A1, 2013 ;

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302
Precautionary Statements : P264-P270-P330

Quality Control

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Computational Chemistry Data

  • TPSA   48.42
  • LogP   1.5302
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   2

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