Ethyl 4-oxo-4H-quinolizine-3-carboxylate

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Reagent Code: #183497
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CAS Number 88612-71-9

science Other reagents with same CAS 88612-71-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.22 g/mol
Formula C₁₂H₁₁NO₃
badge Registry Numbers
MDL Number MFCD04039540
thermostat Physical Properties
Boiling Point 441.9°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a key intermediate in the synthesis of quinolizine-based pharmaceuticals, particularly in the development of antibacterial and antiviral agents. Its structure supports the formation of bioactive molecules that interact with DNA gyrase and topoisomerase enzymes, making it valuable in medicinal chemistry. Also employed in the preparation of fluorescent dyes and optoelectronic materials due to its conjugated aromatic system. Commonly utilized in research settings for generating novel heterocyclic compounds with potential therapeutic activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,930.00
inventory 250mg
10-20 days ฿3,850.00
inventory 1g
10-20 days ฿13,040.00
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Ethyl 4-oxo-4H-quinolizine-3-carboxylate
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Used as a key intermediate in the synthesis of quinolizine-based pharmaceuticals, particularly in the development of antibacterial and antiviral agents. Its structure supports the formation of bioactive molecules that interact with DNA gyrase and topoisomerase enzymes, making it valuable in medicinal chemistry. Also employed in the preparation of fluorescent dyes and optoelectronic materials due to its conjugated aromatic system. Commonly utilized in research settings for generating novel heterocyclic compo
Used as a key intermediate in the synthesis of quinolizine-based pharmaceuticals, particularly in the development of antibacterial and antiviral agents. Its structure supports the formation of bioactive molecules that interact with DNA gyrase and topoisomerase enzymes, making it valuable in medicinal chemistry. Also employed in the preparation of fluorescent dyes and optoelectronic materials due to its conjugated aromatic system. Commonly utilized in research settings for generating novel heterocyclic compounds with potential therapeutic activity.
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