Ethyl 3-bromoimidazo[1,2-a]pyridine-5-carboxylate

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Reagent Code: #45358
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CAS Number 429690-42-6

science Other reagents with same CAS 429690-42-6

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Weight 269.0947 g/mol
Formula C₁₀H₉BrN₂O₂
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MDL Number MFCD10566747
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This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of imidazo[1,2-a]pyridine derivatives. These derivatives are known for their potential therapeutic applications, including antimicrobial, antiviral, and anticancer properties. The bromo and ester functional groups in the molecule make it a versatile building block for further chemical modifications, enabling the creation of diverse compounds for drug discovery and development. Additionally, it is used in the study of structure-activity relationships to optimize the efficacy and selectivity of potential drug candidates.

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inventory 250mg
10-20 days ฿4,212.00

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Ethyl 3-bromoimidazo[1,2-a]pyridine-5-carboxylate
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This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of imidazo[1,2-a]pyridine derivatives. These derivatives are known for their potential therapeutic applications, including antimicrobial, antiviral, and anticancer properties. The bromo and ester functional groups in the molecule make it a versatile building block for further chemical modifications,

This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of imidazo[1,2-a]pyridine derivatives. These derivatives are known for their potential therapeutic applications, including antimicrobial, antiviral, and anticancer properties. The bromo and ester functional groups in the molecule make it a versatile building block for further chemical modifications, enabling the creation of diverse compounds for drug discovery and development. Additionally, it is used in the study of structure-activity relationships to optimize the efficacy and selectivity of potential drug candidates.

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