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Structure of 1227603-42-0
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5-Bromo-2-oxo-1,2-dihydropyridine-3-carbaldehyde features a brominated dihydropyridine core with orthogonal functional groups: a carbonyl at C2 and an aldehyde at C3. This electron-deficient scaffold enables direct coupling in heterocyclic synthesis, serving as a key intermediate for bioactive pyridine derivatives. The molecule exhibits bench-stable handling under standard conditions.
5-Bromo-2-oxo-1,2-dihydropyridine-3-carbaldehyde serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine derivatives via Pd-catalyzed cross-coupling and nucleophilic addition reactions. Its dual functionality—branched bromide and aldehyde groups—facilitates sequential transformations under mild conditions, while the enone system supports conjugate addition pathways. The compound exhibits bench stability and compatibility with common protecting groups, 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: