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Structure of 849807-09-6
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Methyl 2-chloroquinoline-6-carboxylate features a chlorinated quinoline core with a strategically positioned ester group, enabling direct incorporation into heterocyclic synthesis. The electron-deficient quinoline ring facilitates nucleophilic substitution, while the methyl ester serves as a handle for further functionalization. This compound exhibits robust stability under standard bench conditions and demonstrates compatibility with diverse reaction environments in medicinal chemistry and materials science applications.
Methyl 2-chloroquinoline-6-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient construction of quinoline-based scaffolds. The chloro group at the 2-position facilitates nucleophilic substitution, while the ester functionality supports selective transformations under standard conditions. Its bench-stable nature and compatibility with palladium-catalyzed cross-coupling reactions make it well-suited for iterative synthesis of complex heterocyclic systems.
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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: