ethyl 2-chloro-5-fluoroquinoline-3-carboxylate

95%

Reagent Code: #81993
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CAS Number 289654-66-6

science Other reagents with same CAS 289654-66-6

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Weight 253.65 g/mol
Formula C₁₂H₉ClFNO₂
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description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a quinoline core with chloro and fluoro substituents, makes it a valuable building block for developing potential pharmaceutical agents. Researchers often employ it in the design and synthesis of compounds targeting specific enzymes or receptors, particularly in the development of antimicrobial, anticancer, or anti-inflammatory drugs. Additionally, its reactivity allows for further functionalization, enabling the creation of diverse derivatives for structure-activity relationship studies. Its role in drug discovery highlights its importance in advancing therapeutic innovations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,655.00
inventory 250mg
10-20 days ฿23,310.00

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ethyl 2-chloro-5-fluoroquinoline-3-carboxylate
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a quinoline core with chloro and fluoro substituents, makes it a valuable building block for developing potential pharmaceutical agents. Researchers often employ it in the design and synthesis of compounds targeting specific enzymes or receptors, particularly in the development of antimicrobial, anticancer, or anti-inflammatory d

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a quinoline core with chloro and fluoro substituents, makes it a valuable building block for developing potential pharmaceutical agents. Researchers often employ it in the design and synthesis of compounds targeting specific enzymes or receptors, particularly in the development of antimicrobial, anticancer, or anti-inflammatory drugs. Additionally, its reactivity allows for further functionalization, enabling the creation of diverse derivatives for structure-activity relationship studies. Its role in drug discovery highlights its importance in advancing therapeutic innovations.

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