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CS-W001157 4
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2-Chloro-5-iodo-4-methoxypyridine

  • CAS No. 1226878-98-3

  • Cat. No. CS-0150448
  • Molecule weight269.47
  • Purity≥97%
  • MDL No.MFCD18415711

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

2-Chloro-5-iodo-4-methoxypyridine|CS-0150448

Structure of 1226878-98-3

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General Information

  • CAS No. 1226878-98-3
  • Cat. No. CS-0150448
  • Purity ≥97%
  • MDL No. MFCD18415711
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₅ClINO
  • Molecular Weight 269.47
  • Synonym(s) None
  • SMILES COC1=CC(=NC=C1I)Cl

Description

2-Chloro-5-iodo-4-methoxypyridine features a pyridine core functionalized with chlorine, iodine, and methoxy groups at distinct positions, enabling selective cross-coupling reactions. The electron-deficient aromatic ring pairs effectively with palladium catalysts, while the methoxy group enhances solubility and stabilizes intermediates under standard conditions. This compound serves as a key building block in the synthesis of advanced pharmaceuticals and agrochemicals.

Application

2-Chloro-5-iodo-4-methoxypyridine serves as a versatile building block in cross-coupling chemistry, enabling efficient construction of substituted pyridine scaffolds. The chloro and iodo groups provide orthogonal reactivity for Pd-catalyzed coupling reactions, while the methoxy group offers moderate electron-donating character and stability under standard reaction conditions. Its bench-stable nature and compatibility with diverse functional groups facilitate reliable use in medicinal chemistry and process development workflows.

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-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   22.12
  • LogP   2.3482
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   1

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