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CS-W001157 4
Total: USD 88.00

6-Bromo-8-fluoroimidazo[1,2-a]pyridine

  • CAS No. 474709-06-3

  • Cat. No. CS-0037702
  • Purity≥96%
  • MDL No.None

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

6-Bromo-8-fluoroimidazo[1,2-a]pyridine|CS-0037702

Structure of 474709-06-3

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General Information

  • CAS No. 474709-06-3
  • Cat. No. CS-0037702
  • Purity ≥96%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₄BrFN₂
  • Molecular Weight 215.02
  • Synonym(s) None
  • SMILES C1=CN2C=C(C=C(C2=N1)F)Br

Description

6-Bromo-8-fluoroimidazo[1,2-a]pyridine is a heterocyclic scaffold featuring bromo and fluoro substituents at electron-deficient positions, enabling direct functionalization in cross-coupling reactions. This bench-stable, moisture-tolerant building block integrates readily into complex molecular architectures for medicinal chemistry and materials science applications.

Application

6-Bromo-8-fluoroimidazo[1,2-a]pyridine serves as a versatile building block for constructing bioactive heterocycles in medicinal chemistry. Its orthogonal halogenation pattern enables palladium-catalyzed cross-coupling reactions with high efficiency and selectivity. The molecule exhibits excellent bench stability, facilitates straightforward purification, and functions effectively in standard coupling protocols, making it well-suited for the modular synthesis of complex imidazopyridine scaffolds.

Synthesis

  • Route1
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      474709-05-2
    • ~%
    • In-stock
      6-Bromo-8-fluoroimidazo[1,2-a]pyridine|CS-0037702
      474709-06-3

    References

    • Eisai Co., Ltd. Patent: EP1382603 A1, 2004 ; Location in patent: Page 134 ;

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

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Computational Chemistry Data

  • TPSA   17.3
  • LogP   2.2359
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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