7-Bromopyrido[3,2-b]pyrazin-3(4H)-one

95%

  • Product Code: 50192
  CAS:    957107-12-9
Molecular Weight: 226.0302 g./mol Molecular Formula: C₇H₄BrN₃O
EC Number: MDL Number: MFCD18452118
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure makes it a valuable intermediate in the creation of molecules with potential therapeutic properties, especially in the fields of oncology and infectious diseases. Researchers often employ it to develop kinase inhibitors, which are crucial in targeting specific pathways involved in cancer cell proliferation. Additionally, its bromine substituent allows for further functionalization, enabling the creation of diverse chemical libraries for high-throughput screening. This compound is also explored in the design of antimicrobial agents, leveraging its heterocyclic framework to interact with bacterial or viral targets. Its applications are largely confined to laboratory settings, where it serves as a building block for more complex bioactive molecules.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $318.54
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7-Bromopyrido[3,2-b]pyrazin-3(4H)-one
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure makes it a valuable intermediate in the creation of molecules with potential therapeutic properties, especially in the fields of oncology and infectious diseases. Researchers often employ it to develop kinase inhibitors, which are crucial in targeting specific pathways involved in cancer cell proliferation. Additionally, its bromine substituent allows for further functionalization, enabling the creation of diverse chemical libraries for high-throughput screening. This compound is also explored in the design of antimicrobial agents, leveraging its heterocyclic framework to interact with bacterial or viral targets. Its applications are largely confined to laboratory settings, where it serves as a building block for more complex bioactive molecules.
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