Ethyl 4-chloro-6,7-dimethoxyquinoline-3-carboxylate

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Reagent Code: #47179
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CAS Number 26893-14-1

science Other reagents with same CAS 26893-14-1

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Weight 295.7183 g/mol
Formula C₁₄H₁₄ClNO₄
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description Product Description

Ethyl 4-chloro-6,7-dimethoxyquinoline-3-carboxylate is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its quinoline core structure makes it a valuable building block for developing potential therapeutic agents, particularly in the design of antimalarial, anticancer, and antimicrobial drugs. The compound's functional groups, such as the chloro and methoxy substituents, allow for further chemical modifications, enabling researchers to optimize drug candidates for enhanced efficacy and selectivity. Additionally, it has been explored in the development of fluorescent probes and imaging agents due to its inherent photophysical properties. Its versatility in organic synthesis also extends to the creation of novel materials and catalysts for industrial applications.

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inventory 100mg
10-20 days ฿1,683.00

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Ethyl 4-chloro-6,7-dimethoxyquinoline-3-carboxylate
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Ethyl 4-chloro-6,7-dimethoxyquinoline-3-carboxylate is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its quinoline core structure makes it a valuable building block for developing potential therapeutic agents, particularly in the design of antimalarial, anticancer, and antimicrobial drugs. The compound's functional groups, such as the chloro and methoxy substituents, allow for further chemical modifications, enablin

Ethyl 4-chloro-6,7-dimethoxyquinoline-3-carboxylate is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its quinoline core structure makes it a valuable building block for developing potential therapeutic agents, particularly in the design of antimalarial, anticancer, and antimicrobial drugs. The compound's functional groups, such as the chloro and methoxy substituents, allow for further chemical modifications, enabling researchers to optimize drug candidates for enhanced efficacy and selectivity. Additionally, it has been explored in the development of fluorescent probes and imaging agents due to its inherent photophysical properties. Its versatility in organic synthesis also extends to the creation of novel materials and catalysts for industrial applications.

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