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CS-W001157 4
Total: USD 88.00

5-Bromopyrazolo[1,5-a]pyridin-2-amine

  • CAS No. 1507592-34-8

  • Cat. No. CS-0163542
  • Molecule weight212.05
  • Purity≥98%
  • MDL No.MFCD20258723

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

5-Bromopyrazolo[1,5-a]pyridin-2-amine|CS-0163542

Structure of 1507592-34-8

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General Information

  • CAS No. 1507592-34-8
  • Cat. No. CS-0163542
  • Purity ≥98%
  • MDL No. MFCD20258723
  • 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=NN2C=CC(Br)=CC2=C1

Description

5-Bromopyrazolo[1,5-a]pyridin-2-amine features a brominated pyrazolopyridine core with a pendant amine, enabling direct functionalization in cross-coupling and medicinal chemistry. This electron-deficient heterocycle serves as a key scaffold for kinase inhibitors and bioactive compounds, offering high reactivity and stability under standard conditions.

Application

5-Bromopyrazolo[1,5-a]pyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling direct incorporation into biologically active heterocycles. Its bromine atom facilitates palladium-catalyzed cross-coupling reactions, while the pyrazolopyridine core offers favorable metabolic stability and hydrogen-bonding capacity. The amine functionality supports derivatization via acylation or alkylation, enhancing scaffold diversity. This compound exhibits bench stability and compatibility with standard purification methods, making it well-suited for iterative synthesis campaigns in drug discovery programs.

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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