Methyl 6-chloro-4-methylpyridine-3-carboxylate

≥95%

Reagent Code: #205696
label
Alias 6-Chloro-4-methylniacin
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CAS Number 1224464-97-4

science Other reagents with same CAS 1224464-97-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.61 g/mol
Formula C₈H₈ClNO₂
badge Registry Numbers
MDL Number MFCD18258050
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic receptor modulators and other central nervous system agents. It serves as a building block in agrochemicals for developing herbicides and insecticides due to its pyridine core, which enhances bioactivity. Commonly employed in medicinal chemistry for structure-activity relationship studies, especially in optimizing compounds targeting neurological disorders. Its ester and chloro functionalities allow for easy modification through nucleophilic substitution and hydrolysis, enabling diverse derivatization in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿670.00
inventory 500mg
10-20 days ฿3,280.00
inventory 1g
10-20 days ฿4,650.00
inventory 5g
10-20 days ฿19,540.00
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Methyl 6-chloro-4-methylpyridine-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic receptor modulators and other central nervous system agents. It serves as a building block in agrochemicals for developing herbicides and insecticides due to its pyridine core, which enhances bioactivity. Commonly employed in medicinal chemistry for structure-activity relationship studies, especially in optimizing compounds targeting neurological disorders. Its ester and chloro functionalities allo

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic receptor modulators and other central nervous system agents. It serves as a building block in agrochemicals for developing herbicides and insecticides due to its pyridine core, which enhances bioactivity. Commonly employed in medicinal chemistry for structure-activity relationship studies, especially in optimizing compounds targeting neurological disorders. Its ester and chloro functionalities allow for easy modification through nucleophilic substitution and hydrolysis, enabling diverse derivatization in drug discovery programs.

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