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CS-W001157 4
Total: USD 88.00

2-Bromo-5-chloropyridine-4-carboxylic acid

  • CAS No. 530156-90-2

  • Cat. No. CS-D0157
  • Purity≥97%
  • MDL No.MFCD13181649

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

2-Bromo-5-chloropyridine-4-carboxylic acid|CS-D0157

Structure of 530156-90-2

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General Information

  • CAS No. 530156-90-2
  • Cat. No. CS-D0157
  • Purity ≥97%
  • MDL No. MFCD13181649
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₃BrClNO₂
  • Molecular Weight 236.45
  • Synonym(s) 2-Bromo-5-chloroisonicotinic acid
  • SMILES O=C(C1=CC(Br)=NC=C1Cl)O

Description

2-Bromo-5-chloropyridine-4-carboxylic acid features a pyridine core functionalized with bromo, chloro, and carboxylic acid groups at the 2, 5, and 4 positions respectively. This tri-substituted heterocycle combines halogen reactivity with an acidic handle, enabling direct coupling or derivatization in cross-coupling reactions and medicinal chemistry workflows. The electron-deficient aromatic system enhances regioselectivity in palladium-catalyzed transformations.

Application

2-Bromo-5-chloropyridine-4-carboxylic acid serves as a versatile building block for the synthesis of substituted pyridine derivatives, enabling efficient functionalization via cross-coupling reactions. Its orthogonal halogenation pattern facilitates selective transformations at the bromo or chloro positions, while the carboxylic acid group supports direct derivatization or incorporation into heterocyclic scaffolds. The compound exhibits good bench stability and compatibility with standard reaction conditions, making it well-suited for medicinal chemistry and process development 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

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Computational Chemistry Data

  • TPSA   50.19
  • LogP   2.1957
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   1

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