Ethyl 4-oxo-1,4-dihydroquinoline-3-carboxylate

98%

Reagent Code: #182919
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CAS Number 52980-28-6

science Other reagents with same CAS 52980-28-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.22 g/mol
Formula C₁₂H₁₁NO₃
thermostat Physical Properties
Melting Point 270°C
Boiling Point 343.7°C
inventory_2 Storage & Handling
Density 1.246g/mL
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolone drugs which exhibit broad-spectrum antibacterial activity. Its structure allows for functionalization at multiple sites, enabling the development of derivatives with enhanced pharmacokinetic properties and improved efficacy against resistant bacterial strains. Also employed in medicinal chemistry research for the design of novel heterocyclic compounds with potential anticancer, antiviral, and anti-inflammatory activities. Its keto and ester functionalities make it suitable for condensation and coupling reactions in organic synthesis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿790.00
inventory 5g
10-20 days ฿2,450.00
inventory 25g
10-20 days ฿9,770.00

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Ethyl 4-oxo-1,4-dihydroquinoline-3-carboxylate
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Used as a key intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolone drugs which exhibit broad-spectrum antibacterial activity. Its structure allows for functionalization at multiple sites, enabling the development of derivatives with enhanced pharmacokinetic properties and improved efficacy against resistant bacterial strains. Also employed in medicinal chemistry research for the design of novel heterocyclic compounds with potential anticancer, antivira

Used as a key intermediate in the synthesis of quinolone antibiotics, particularly in the production of fluoroquinolone drugs which exhibit broad-spectrum antibacterial activity. Its structure allows for functionalization at multiple sites, enabling the development of derivatives with enhanced pharmacokinetic properties and improved efficacy against resistant bacterial strains. Also employed in medicinal chemistry research for the design of novel heterocyclic compounds with potential anticancer, antiviral, and anti-inflammatory activities. Its keto and ester functionalities make it suitable for condensation and coupling reactions in organic synthesis.

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