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CS-W001157 4
Total: USD 88.00

3-Bromoimidazo[1,2-b]pyridazine

  • CAS No. 18087-73-5

  • Cat. No. CS-W019836
  • Molecule weight198.02
  • Purity≥98%
  • MDL No.MFCD09757672

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

3-Bromoimidazo[1,2-b]pyridazine|CS-W019836

Structure of 18087-73-5

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General Information

  • CAS No. 18087-73-5
  • Cat. No. CS-W019836
  • Purity ≥98%
  • MDL No. MFCD09757672
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₄BrN₃
  • Molecular Weight 198.02
  • Synonym(s) 3-bromo-imidazo[1,2-b]pyridazine
  • SMILES BrC1=CN=C2C=CC=NN21

Description

3-Bromoimidazo[1,2-b]pyridazine is a brominated heterocyclic compound featuring a fused imidazo[1,2-b]pyridazine core. This electron-deficient scaffold enables direct functionalization in cross-coupling reactions. The bromine substituent provides a reactive handle for palladium-catalyzed transformations, facilitating rapid access to diverse analogs in medicinal chemistry and materials science applications.

Application

3-Bromoimidazo[1,2-b]pyridazine serves as a versatile building block for medicinal chemistry and heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions with high functional group tolerance. Its bromine substituent facilitates efficient C–C and C–heteroatom bond formation under standard conditions, while the imidazo[1,2-b]pyridazine core provides a rigid, electron-deficient scaffold useful in kinase inhibitor and CNS-targeted compound development. The compound exhibits excellent bench stability and simplifies purification in multi-step syntheses.

Synthesis

  • Route1

    References

    • Stanovnik, Branko; Tisler, Miha; Drnovsek, Iztok Synthesis, 1981 , # 12 p. 987 - 989

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 : H315
Precautionary Statements : P264-P280-P302+P352-P332+P313-P362+P364

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Computational Chemistry Data

  • TPSA   30.19
  • LogP   1.4918
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   0

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