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Structure of 51355-94-3
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6-Bromopyridazin-3(2H)-one delivers a brominated pyridazinone scaffold with enhanced reactivity at the C6 position, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. The lactam carbonyl group provides polarity and hydrogen-bonding capacity, improving solubility in polar solvents and compatibility with diverse synthetic workflows. This bench-stable heterocycle serves as a key intermediate for bioactive molecule construction.
6-Bromopyridazin-3(2H)-one serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The bromine substituent exhibits high reactivity in Suzuki, Stille, and Negishi couplings, while the pyridazinone core provides excellent stability and solubility in common organic solvents. Its well-defined electronic profile supports predictable reactivity, facilitating rapid diversification of heterocyclic scaffolds for drug discovery 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-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: