Ethyl 4-bromoquinoline-3-carboxylate

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Reagent Code: #47564
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CAS Number 1242260-12-3

science Other reagents with same CAS 1242260-12-3

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Weight 280.1173 g/mol
Formula C₁₂H₁₀BrNO₂
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Ethyl 4-bromoquinoline-3-carboxylate is primarily utilized in organic synthesis as a key intermediate for the development of various biologically active compounds. It serves as a building block in the synthesis of quinoline derivatives, which are known for their pharmacological properties, including antimicrobial, anticancer, and anti-inflammatory activities. Additionally, this compound is employed in the preparation of fluorescent dyes and imaging agents due to its quinoline core, which can be modified to exhibit photophysical properties. Its bromo and ester functional groups make it a versatile reagent for further chemical transformations, such as cross-coupling reactions, enabling the creation of complex molecular structures in medicinal chemistry and materials science.

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inventory 250mg
10-20 days ฿1,368.00

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Ethyl 4-bromoquinoline-3-carboxylate
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Ethyl 4-bromoquinoline-3-carboxylate is primarily utilized in organic synthesis as a key intermediate for the development of various biologically active compounds. It serves as a building block in the synthesis of quinoline derivatives, which are known for their pharmacological properties, including antimicrobial, anticancer, and anti-inflammatory activities. Additionally, this compound is employed in the preparation of fluorescent dyes and imaging agents due to its quinoline core, which can be modified

Ethyl 4-bromoquinoline-3-carboxylate is primarily utilized in organic synthesis as a key intermediate for the development of various biologically active compounds. It serves as a building block in the synthesis of quinoline derivatives, which are known for their pharmacological properties, including antimicrobial, anticancer, and anti-inflammatory activities. Additionally, this compound is employed in the preparation of fluorescent dyes and imaging agents due to its quinoline core, which can be modified to exhibit photophysical properties. Its bromo and ester functional groups make it a versatile reagent for further chemical transformations, such as cross-coupling reactions, enabling the creation of complex molecular structures in medicinal chemistry and materials science.

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