Ethyl 4-chloro-8-nitroquinoline-3-carboxylate

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Reagent Code: #184540
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CAS Number 131548-98-6

science Other reagents with same CAS 131548-98-6

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Weight 280.66 g/mol
Formula C₁₂H₉ClN₂O₄
badge Registry Numbers
MDL Number MFCD18251635
inventory_2 Storage & Handling
Density 1.439 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of quinolone-based pharmaceuticals, particularly in the development of antimicrobial and antitumor agents. Its structure supports the construction of bioactive molecules by enabling further functionalization at key positions on the quinoline ring. Commonly employed in research settings for designing novel compounds with potential activity against resistant bacterial strains and certain cancer cell lines. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its electron-withdrawing nitro and chloro substituents, which influence reactivity and binding affinity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,670.00
inventory 250mg
10-20 days ฿15,420.00
inventory 1g
10-20 days ฿40,020.00

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Ethyl 4-chloro-8-nitroquinoline-3-carboxylate
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Used as an intermediate in the synthesis of quinolone-based pharmaceuticals, particularly in the development of antimicrobial and antitumor agents. Its structure supports the construction of bioactive molecules by enabling further functionalization at key positions on the quinoline ring. Commonly employed in research settings for designing novel compounds with potential activity against resistant bacterial strains and certain cancer cell lines. Also utilized in medicinal chemistry for structure-activity

Used as an intermediate in the synthesis of quinolone-based pharmaceuticals, particularly in the development of antimicrobial and antitumor agents. Its structure supports the construction of bioactive molecules by enabling further functionalization at key positions on the quinoline ring. Commonly employed in research settings for designing novel compounds with potential activity against resistant bacterial strains and certain cancer cell lines. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its electron-withdrawing nitro and chloro substituents, which influence reactivity and binding affinity.

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