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CS-W001157 4
Total: USD 88.00

6-Bromo-7-chloroimidazo[1,2-a]pyridine

  • CAS No. 1303890-45-0

  • Cat. No. CS-0102567
  • Molecule weight231.48
  • Purity≥97%
  • MDL No.None

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

6-Bromo-7-chloroimidazo[1,2-a]pyridine|CS-0102567

Structure of 1303890-45-0

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General Information

  • CAS No. 1303890-45-0
  • Cat. No. CS-0102567
  • Purity ≥97%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₄BrClN₂
  • Molecular Weight 231.48
  • Synonym(s) IMidazo[1,2-a]pyridine, 6-broMo-7-chloro-
  • SMILES ClC1=CC2=NC=CN2C=C1Br

Description

6-Bromo-7-chloroimidazo[1,2-a]pyridine features a fused heterocyclic core with complementary halogen substituents at the 6- and 7-positions, enabling selective cross-coupling reactions. The electron-deficient pyridine ring enhances reactivity in palladium-catalyzed transformations, while the sterically accessible framework supports efficient functionalization. This scaffold serves as a key building block for bioactive imidazopyridine derivatives in medicinal chemistry.

Application

6-Bromo-7-chloroimidazo[1,2-a]pyridine serves as a versatile building block in medicinal chemistry, enabling the construction of imidazo[1,2-a]pyridine scaffolds via palladium-catalyzed cross-coupling reactions. Its dual halogenation pattern supports sequential functionalization, offering orthogonal reactivity for C–C and C–heteroatom bond formation. The compound exhibits excellent bench stability and facilitates efficient purification, making it well-suited for scalable synthesis of bioactive heterocycles.

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-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   17.3
  • LogP   2.7502
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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