methyl 2-cyclopropyl-4-(4-fluorophenyl)quinoline-3-carboxylate

98%

Reagent Code: #128451
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CAS Number 121659-86-7

science Other reagents with same CAS 121659-86-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 321.34 g/mol
Formula C₂₀H₁₆FNO₂
badge Registry Numbers
MDL Number MFCD11041028
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of quinoline-based pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its structure allows for selective interactions with biological targets, making it valuable in medicinal chemistry research. The presence of fluorophenyl and cyclopropyl groups enhances metabolic stability and binding affinity in drug candidates. Commonly employed in structure-activity relationship (SAR) studies to optimize potency and pharmacokinetic properties. Also utilized in the preparation of kinase inhibitors and antimicrobial agents in preclinical drug discovery.

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Test Parameter Specification
Appearance Pale Yellow to Light Yellow Solid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿25,000.00

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methyl 2-cyclopropyl-4-(4-fluorophenyl)quinoline-3-carboxylate
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Used as a key intermediate in the synthesis of quinoline-based pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its structure allows for selective interactions with biological targets, making it valuable in medicinal chemistry research. The presence of fluorophenyl and cyclopropyl groups enhances metabolic stability and binding affinity in drug candidates. Commonly employed in structure-activity relationship (SAR) studies to optimize potency and pharmacokin

Used as a key intermediate in the synthesis of quinoline-based pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its structure allows for selective interactions with biological targets, making it valuable in medicinal chemistry research. The presence of fluorophenyl and cyclopropyl groups enhances metabolic stability and binding affinity in drug candidates. Commonly employed in structure-activity relationship (SAR) studies to optimize potency and pharmacokinetic properties. Also utilized in the preparation of kinase inhibitors and antimicrobial agents in preclinical drug discovery.

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