Ethyl 2-methylquinoline-6-carboxylate

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Reagent Code: #183560
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CAS Number 855763-77-8

science Other reagents with same CAS 855763-77-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.25 g/mol
Formula C₁₃H₁₃NO₂
badge Registry Numbers
MDL Number MFCD09879697
thermostat Physical Properties
Boiling Point 334.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial drugs. Its structure supports the formation of quinoline-based active compounds that exhibit biological activity against Plasmodium species. Also employed in research settings for the preparation of fluorescent dyes and sensors due to the inherent photophysical properties of the quinoline core. The ester group allows for easy functionalization, making it valuable in organic synthesis and medicinal chemistry for building more complex molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿790.00
inventory 1g
10-20 days ฿2,020.00
inventory 10g
10-20 days ฿10,140.00
inventory 5g
10-20 days ฿5,640.00
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Ethyl 2-methylquinoline-6-carboxylate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial drugs. Its structure supports the formation of quinoline-based active compounds that exhibit biological activity against Plasmodium species. Also employed in research settings for the preparation of fluorescent dyes and sensors due to the inherent photophysical properties of the quinoline core. The ester group allows for easy functionalization, making it valuable in organic synthesis and medicinal

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial drugs. Its structure supports the formation of quinoline-based active compounds that exhibit biological activity against Plasmodium species. Also employed in research settings for the preparation of fluorescent dyes and sensors due to the inherent photophysical properties of the quinoline core. The ester group allows for easy functionalization, making it valuable in organic synthesis and medicinal chemistry for building more complex molecules.

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