Ethyl 4-ethoxypicolinate

97%

Reagent Code: #182449
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CAS Number 71777-70-3

science Other reagents with same CAS 71777-70-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.22 g/mol
Formula C₁₀H₁₃NO₃
thermostat Physical Properties
Boiling Point 309°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and other central nervous system agents. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building pyridine-based drug candidates. It is also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance binding selectivity in biologically active molecules. Commonly utilized in cross-coupling reactions and ester transformations during route scouting in process chemistry.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿430.00
inventory 100mg
10-20 days ฿700.00

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Ethyl 4-ethoxypicolinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and other central nervous system agents. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building pyridine-based drug candidates. It is also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance binding selectivity in biologically active molecules. Commonly utiliz

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and other central nervous system agents. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building pyridine-based drug candidates. It is also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance binding selectivity in biologically active molecules. Commonly utilized in cross-coupling reactions and ester transformations during route scouting in process chemistry.

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