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CS-W001157 4
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5-Bromoimidazo[1,2-a]pyridin-2-amine

  • CAS No. 1350738-82-7

  • Cat. No. CS-0056792
  • Purity≥98%
  • MDL No.MFCD20502277

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

5-Bromoimidazo[1,2-a]pyridin-2-amine|CS-0056792

Structure of 1350738-82-7

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General Information

  • CAS No. 1350738-82-7
  • Cat. No. CS-0056792
  • Purity ≥98%
  • MDL No. MFCD20502277
  • 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=CN2C(Br)=CC=CC2=N1

Description

5-Bromoimidazo[1,2-a]pyridin-2-amine features a fused heterocyclic core with a bromine atom at the 5-position and an amine group at the 2-position, enabling direct functionalization in cross-coupling reactions. This electron-deficient scaffold integrates readily into bioactive molecules, offering high reactivity and stability under standard conditions.

Application

5-Bromoimidazo[1,2-a]pyridin-2-amine serves as a versatile building block for heterocyclic synthesis, enabling efficient access to imidazo[1,2-a]pyridine-based scaffolds prevalent in medicinal chemistry. Its bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the amine functionality supports derivatization via acylation, alkylation, or coupling protocols. The compound exhibits good bench stability and is readily purified by chromatography, making it well-suited for iterative synthesis campaigns in API development.

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

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