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Structure of 120034-05-1
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Methyl 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylate features a brominated dihydropyridine core with orthogonal functional groups enabling direct coupling in heterocyclic synthesis. The electron-deficient pyridine ring facilitates nucleophilic substitution, while the ester moiety supports derivatization under mild conditions. This bench-stable reagent streamlines access to complex nitrogen-containing scaffolds in medicinal chemistry and materials science.
Methyl 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds. The bromo group facilitates palladium-catalyzed coupling reactions, while the ester and enone functionalities support further functionalization via nucleophilic addition or reduction. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for iterative synthesis in 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 : 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: