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Structure of 32383-03-2
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2,3-Dimethyl 6-chloropyridine-2,3-dicarboxylate features a pyridine core functionalized with chlorine at C6 and ester groups at C2 and C3, flanked by methyl substituents. This electron-deficient heterocycle integrates readily into transition-metal-catalyzed couplings and serves as a key scaffold in medicinal chemistry for constructing bioactive molecules under standard conditions.
2,3-Dimethyl 6-chloropyridine-2,3-dicarboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds via cross-coupling and nucleophilic substitution reactions. The presence of orthogonal ester groups and a reactive chloro substituent facilitates sequential functionalization. Its bench-stable crystalline form supports straightforward handling and purification, making it well-suited for iterative synthetic strategies in medicinal chemistry and process development.
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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: