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Structure of 1186637-40-0
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This 3-bromo-6-oxo-1,6-dihydropyridine-2-carbonitrile features a reactive pyridine core with complementary electron-withdrawing groups: a cyano function at C2 and a ketone at C6. The bromine substituent at C3 enables facile cross-coupling reactions, making this scaffold valuable for constructing diverse heterocyclic architectures in medicinal chemistry and materials science.
3-Bromo-6-oxo-1,6-dihydropyridine-2-carbonitrile serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted pyridine derivatives via palladium-catalyzed cross-coupling and nucleophilic substitution reactions. The molecule combines a reactive bromide with a conjugated enone system and an electron-withdrawing nitrile group, facilitating orthogonal functionalization and stable handling under standard laboratory conditions. Its structural motif is well-suited for constructing bioactive scaffolds in medicinal chemistry 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: