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CS-W001157 4
Total: USD 88.00

7-Bromoimidazo[1,2-a]pyridin-3-amine

  • CAS No. 1427439-69-7

  • Cat. No. CS-0214447
  • Purity≥96%
  • MDL No.None

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

7-Bromoimidazo[1,2-a]pyridin-3-amine|CS-0214447

Structure of 1427439-69-7

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General Information

  • CAS No. 1427439-69-7
  • Cat. No. CS-0214447
  • Purity ≥96%
  • MDL No. None
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₆BrN₃
  • Molecular Weight 212.05
  • Synonym(s) None
  • SMILES NC1=CN=C2C=C(Br)C=CN21

Description

7-Bromoimidazo[1,2-a]pyridin-3-amine serves as a versatile heterocyclic scaffold for medicinal chemistry and catalysis. The bromo substituent enables palladium-catalyzed cross-coupling reactions, while the imidazopyridine core offers enhanced metabolic stability and favorable binding interactions in kinase-targeted drug discovery.

Application

7-Bromoimidazo[1,2-a]pyridin-3-amine serves as a versatile building block for medicinal chemistry and catalytic cross-coupling applications. The bromo group enables palladium-catalyzed transformations such as Suzuki-Miyaura and Buchwald-Hartwig couplings, while the imidazo[1,2-a]pyridine core provides a rigid, electron-deficient heterocyclic scaffold with favorable pharmacokinetic properties. Bench-stable and readily purified by flash chromatography, it facilitates efficient access to complex nitrogen-containing architectures in drug discovery campaigns.

Safety Information

Download SDS
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-P362+P364-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   43.32
  • LogP   1.679
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   0

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