7-Bromopyrido[3,2-b]pyrazin-3(4H)-one
95%
Reagent
Code: #50192
CAS Number
957107-12-9
blur_circular Chemical Specifications
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Molecular Information
Weight
226.0302 g/mol
Formula
C₇H₄BrN₃O
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Registry Numbers
MDL Number
MFCD18452118
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Storage & Handling
Storage
room temperature
description 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.
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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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