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CS-W001157 4
Total: USD 88.00

2-Chloro-6-methoxy-4-methylpyridine

  • CAS No. 25297-52-3

  • Cat. No. CS-W007131
  • Purity≥97%
  • MDL No.MFCD16610595

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

2-Chloro-6-methoxy-4-methylpyridine|CS-W007131

Structure of 25297-52-3

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General Information

  • CAS No. 25297-52-3
  • Cat. No. CS-W007131
  • Purity ≥97%
  • MDL No. MFCD16610595
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₈ClNO
  • Molecular Weight 157.60
  • Synonym(s) Pyridine, 2-chloro-6-Methoxy-4-Methyl-
  • SMILES CC1=CC(Cl)=NC(OC)=C1

Description

2-Chloro-6-methoxy-4-methylpyridine features a pyridine core functionalized with chlorine, methoxy, and methyl groups at the 2-, 6-, and 4-positions respectively. This electron-deficient heterocycle serves as a key intermediate in medicinal chemistry, enabling direct coupling reactions due to its regioselective reactivity. The methoxy group enhances solubility and modulates electronic properties, while the methyl substituent adds steric bulk. The compound exhibits bench-stable handling under standard conditions.

Application

2-Chloro-6-methoxy-4-methylpyridine serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The ortho-chloro group facilitates selective substitution, while the methoxy and methyl substituents provide steric and electronic modulation. Its bench stability and compatibility with diverse reaction conditions make it well-suited for constructing complex heterocyclic scaffolds in API development.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H227-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   22.12
  • LogP   2.05202
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   1

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