Ethyl 6-bromo-5-methylimidazo[1,2-a]pyridine-2-carboxylate

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Reagent Code: #49950
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CAS Number 859787-40-9

science Other reagents with same CAS 859787-40-9

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Weight 283.12 g/mol
Formula C₁₁H₁₁BrN₂O₂
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MDL Number MFCD19105298
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring an imidazopyridine core, makes it a valuable intermediate for creating molecules with potential therapeutic applications. Researchers often employ it in the design of compounds targeting neurological disorders, such as anxiety, insomnia, and epilepsy, due to its ability to interact with specific receptors in the brain. Additionally, its bromo and ester functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for biological screening and optimization in drug discovery programs.

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inventory 250mg
10-20 days ฿1,503.00

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Ethyl 6-bromo-5-methylimidazo[1,2-a]pyridine-2-carboxylate
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring an imidazopyridine core, makes it a valuable intermediate for creating molecules with potential therapeutic applications. Researchers often employ it in the design of compounds targeting neurological disorders, such as anxiety, insomnia, and epilepsy, due to its ability to interact with specific receptors in the brain. Additionally, its bromo and

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring an imidazopyridine core, makes it a valuable intermediate for creating molecules with potential therapeutic applications. Researchers often employ it in the design of compounds targeting neurological disorders, such as anxiety, insomnia, and epilepsy, due to its ability to interact with specific receptors in the brain. Additionally, its bromo and ester functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for biological screening and optimization in drug discovery programs.

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