Ethyl 4-chloro-2-oxo-1,2-dihydroquinoline-3-carboxylate

95%

Reagent Code: #185421
fingerprint
CAS Number 99429-64-8

science Other reagents with same CAS 99429-64-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.67 g/mol
Formula C₁₂H₁₀ClNO₃
badge Registry Numbers
MDL Number MFCD00572655
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Widely used as a key intermediate in the synthesis of quinolone-based pharmaceuticals, particularly in the development of antibacterial agents. Its structure supports the formation of fluorinated quinolones, which are critical for enhancing antimicrobial potency and broadening the spectrum of activity. Commonly employed in medicinal chemistry for constructing the core scaffold of drugs targeting DNA gyrase and topoisomerase IV. Also utilized in research settings for generating novel heterocyclic compounds with potential therapeutic applications in oncology and anti-inflammatory treatments. Its ester and carbonyl functionalities allow for easy modification, making it valuable in combinatorial chemistry and drug discovery pipelines.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,100.00
inventory 250mg
10-20 days ฿1,930.00
inventory 1g
10-20 days ฿7,140.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl 4-chloro-2-oxo-1,2-dihydroquinoline-3-carboxylate
No image available
Widely used as a key intermediate in the synthesis of quinolone-based pharmaceuticals, particularly in the development of antibacterial agents. Its structure supports the formation of fluorinated quinolones, which are critical for enhancing antimicrobial potency and broadening the spectrum of activity. Commonly employed in medicinal chemistry for constructing the core scaffold of drugs targeting DNA gyrase and topoisomerase IV. Also utilized in research settings for generating novel heterocyclic compounds with potential therapeutic applications in oncology and anti-inflammatory treatments. Its ester and carbonyl functionalities allow for easy modification, making it valuable in combinatorial chemistry and drug discovery pipelines.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...