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Structure of 103502-48-3
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Methyl 2-bromoquinoline-4-carboxylate is a bench-stable, moisture-tolerant heterocyclic building block featuring a brominated quinoline core paired with an ester-functionalized C4 position. This compound integrates readily into cross-coupling reactions and serves as a key intermediate in the synthesis of bioactive quinoline derivatives for medicinal chemistry applications.
Methyl 2-bromoquinoline-4-carboxylate serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-established reactivity at the C2 position. The quinoline scaffold provides inherent stability and favorable electronic properties for further functionalization, while the ester group allows for selective derivatization. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient synthesis of complex heterocyclic systems and API intermediates.
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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: