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Structure of 137520-99-1
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Ethyl 2,6-dichloro-3-methylpyridine-4-carboxylate features a sterically hindered pyridine core with electron-withdrawing chloro groups flanking a methyl-substituted position. This configuration enhances regioselectivity in cross-coupling reactions and provides stability under standard bench conditions. The ester functionality enables direct incorporation into complex heterocyclic architectures without additional protection.
Ethyl 2,6-dichloro-3-methylpyridine-4-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds via cross-coupling and nucleophilic substitution reactions. The dichloro substitution pattern facilitates selective functionalization, while the ester group supports subsequent transformations. Bench-stable and compatible with standard reaction conditions, it functions effectively in medicinal chemistry and agrochemical research workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: