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8-Bromo-3-iodoimidazo[1,2-a]pyridine

  • CAS No. 1232038-69-5

  • Cat. No. CS-0155564
  • Molecule weightNone
  • Purity≥97%
  • MDL No.MFCD22627990

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

8-Bromo-3-iodoimidazo[1,2-a]pyridine|CS-0155564

Structure of 1232038-69-5

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General Information

  • CAS No. 1232038-69-5
  • Cat. No. CS-0155564
  • Purity ≥97%
  • MDL No. MFCD22627990
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₄BrIN₂
  • Molecular Weight None
  • Synonym(s) 8-BroMo-3-iodo-iMidazo[1,2-a]pyridine
  • SMILES C1=CN2C(=CN=C2C(=C1)Br)I

Description

8-Bromo-3-iodoimidazo[1,2-a]pyridine features a fused heterocyclic core with complementary halogen handles at the 8-bromo and 3-iodo positions. This configuration enables selective cross-coupling reactions under palladium catalysis, facilitating efficient access to complex imidazopyridine architectures in medicinal chemistry and materials synthesis. The molecule exhibits excellent stability under standard reaction conditions.

Application

8-Bromo-3-iodoimidazo[1,2-a]pyridine serves as a versatile building block for constructing complex heterocyclic scaffolds in medicinal chemistry and catalysis research. The molecule features orthogonal halogen handles—bromine at C8 and iodine at C3—that enable sequential cross-coupling reactions under palladium-catalyzed conditions. Its bench-stable crystalline form facilitates handling and purification, while the electron-deficient imidazopyridine core supports diverse functionalization, making it well-suited for targeted synthesis of bioactive compounds and catalyst precursors.

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-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P405-P501

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Computational Chemistry Data

  • TPSA   17.3
  • LogP   2.7014
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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