Ethyl 4-hydroxy-1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxylate

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Reagent Code: #185332
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CAS Number 57513-54-9

science Other reagents with same CAS 57513-54-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.25 g/mol
Formula C₁₃H₁₃NO₄
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MDL Number MFCD00117242
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

This compound serves as a valuable intermediate in the synthesis of quinolone derivatives, particularly for pharmaceutical applications such as antibacterial and antiviral agents. Its heterocyclic quinoline structure facilitates chemical modifications to create bioactive molecules with potential antimicrobial, anti-inflammatory, and antioxidant properties. It is commonly used in medicinal chemistry research to develop novel therapeutic compounds. Additionally, due to its conjugated aromatic system, it acts as a building block for fluorescent dyes and luminescent materials that exhibit fluorescence under UV light.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,990.00

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Ethyl 4-hydroxy-1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxylate
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This compound serves as a valuable intermediate in the synthesis of quinolone derivatives, particularly for pharmaceutical applications such as antibacterial and antiviral agents. Its heterocyclic quinoline structure facilitates chemical modifications to create bioactive molecules with potential antimicrobial, anti-inflammatory, and antioxidant properties. It is commonly used in medicinal chemistry research to develop novel therapeutic compounds. Additionally, due to its conjugated aromatic system, it ac

This compound serves as a valuable intermediate in the synthesis of quinolone derivatives, particularly for pharmaceutical applications such as antibacterial and antiviral agents. Its heterocyclic quinoline structure facilitates chemical modifications to create bioactive molecules with potential antimicrobial, anti-inflammatory, and antioxidant properties. It is commonly used in medicinal chemistry research to develop novel therapeutic compounds. Additionally, due to its conjugated aromatic system, it acts as a building block for fluorescent dyes and luminescent materials that exhibit fluorescence under UV light.

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