Ethyl 2-chloro-6-methylpyridine-4-carboxylate

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Reagent Code: #181852
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Alias Ethyl 2-chloro-6-methyl-4-picolinic acid; Ethyl 2-chloro-6-methylpyridin-4-carboxylic acid
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CAS Number 3998-88-7

science Other reagents with same CAS 3998-88-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.63 g/mol
Formula C₉H₁₀ClNO₂
thermostat Physical Properties
Melting Point 65-67°C
Boiling Point 107°C at 1.5 mmHg
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly in the production of herbicides and insecticides. Its structure allows for functionalization in pesticide active ingredients, enhancing selectivity and efficacy. Also employed in pharmaceutical research for building pyridine-based drug candidates, especially those targeting central nervous system disorders. The ester and chloro groups enable further chemical modifications, making it valuable in organic synthesis and development of novel bioactive compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿320.00
inventory 5g
10-20 days ฿3,530.00

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Ethyl 2-chloro-6-methylpyridine-4-carboxylate
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Used as a key intermediate in the synthesis of agrochemicals, particularly in the production of herbicides and insecticides. Its structure allows for functionalization in pesticide active ingredients, enhancing selectivity and efficacy. Also employed in pharmaceutical research for building pyridine-based drug candidates, especially those targeting central nervous system disorders. The ester and chloro groups enable further chemical modifications, making it valuable in organic synthesis and development of

Used as a key intermediate in the synthesis of agrochemicals, particularly in the production of herbicides and insecticides. Its structure allows for functionalization in pesticide active ingredients, enhancing selectivity and efficacy. Also employed in pharmaceutical research for building pyridine-based drug candidates, especially those targeting central nervous system disorders. The ester and chloro groups enable further chemical modifications, making it valuable in organic synthesis and development of novel bioactive compounds.

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