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CS-W001157 4
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5-Bromo-2-chloro-4-iodopyridine

  • CAS No. 401892-47-5

  • Cat. No. CS-0135792
  • Purity≥97%
  • MDL No.MFCD09972189

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

5-Bromo-2-chloro-4-iodopyridine|CS-0135792

Structure of 401892-47-5

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General Information

  • CAS No. 401892-47-5
  • Cat. No. CS-0135792
  • Purity ≥97%
  • MDL No. MFCD09972189
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₂BrClIN
  • Molecular Weight 318.34
  • Synonym(s) 5-bromo-4-iodo-2-chloropyridine
  • SMILES IC1=CC(Cl)=NC=C1Br

Description

5-Bromo-2-chloro-4-iodopyridine features a trihalogenated pyridine core with distinct halogen positions enabling selective cross-coupling reactions. The strategic placement of bromo, chloro, and iodo substituents supports sequential functionalization in transition-metal-catalyzed processes. This molecule delivers high reactivity and orthogonal handle compatibility for complex heterocyclic synthesis under standard conditions.

Application

5-Bromo-2-chloro-4-iodopyridine serves as a versatile trihalogenated pyridine building block for transition-metal-catalyzed cross-coupling reactions. Its orthogonal halogen reactivity enables sequential functionalization at distinct positions, facilitating the construction of complex heterocyclic scaffolds. The molecule exhibits excellent bench stability and compatibility with palladium-catalyzed coupling protocols, making it ideal for iterative synthesis in medicinal chemistry and agrochemical research.

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-P280-P302+P352

Quality Control

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Computational Chemistry Data

  • TPSA   12.89
  • LogP   3.1021
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   0

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