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Structure of 1780045-62-6
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This electron-deficient dihydropyridine scaffold features a bromo group at C5 and a nitrile-bearing carbonyl at C6, enabling direct functionalization in cross-coupling and cycloaddition reactions. The fused heterocyclic core delivers high reactivity under mild conditions, supporting rapid access to complex nitrogen-containing architectures in medicinal chemistry and materials synthesis.
5-Bromo-6-oxo-1,6-dihydropyridine-2-carbonitrile serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds. The molecule combines a bromo substituent for late-stage functionalization, a readily reducible ketone, and a nitrile group compatible with nucleophilic addition and cyclization reactions. Its bench-stable nature and tolerance to common reaction conditions facilitate integration into multi-step synthetic sequences for medicinal chemistry and materials science applications.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: