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Structure of 98786-86-8
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3-Amino-5-bromopyridin-2(1H)-one features a brominated pyridinone core with an amino group at the 3-position, enabling direct functionalization in cross-coupling and heterocycle synthesis. The molecule exhibits enhanced solubility and stability under standard conditions, facilitating use in medicinal chemistry workflows and as a building block for bioactive compounds.
3-Amino-5-bromopyridin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the amino and bromo positions. The compound exhibits good bench stability and facilitates palladium-catalyzed cross-coupling reactions, including Suzuki-Miyaura and Buchwald-Hartwig couplings. Its dual reactive handles support efficient construction of complex heterocyclic scaffolds, particularly in kinase inhibitor and CNS-targeted drug discovery programs.
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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: