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Structure of 206257-39-8
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Ethyl 6-bromo-4-chloroquinoline-3-carboxylate features a fused quinoline core with complementary halogen handles at the 6-bromo and 4-chloro positions, enabling selective cross-coupling reactions. This bench-stable derivative integrates readily into diverse synthetic sequences requiring dual electrophilic sites, particularly in medicinal chemistry and materials science applications where precise functionalization is critical.
Ethyl 6-bromo-4-chloroquinoline-3-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen functionality. The 6-bromo and 4-chloro substituents facilitate sequential functionalization, while the ester group supports further transformations. This compound exhibits excellent bench stability and is readily purified by standard chromatographic methods, making it well-suited for medicinal chemistry and process development 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 : H319
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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: