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Structure of 879488-53-6
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1-(6-Bromopyridin-3-yl)-4-methylpiperazine features a brominated pyridine moiety paired with a sterically hindered piperazine ring, enabling direct functionalization in late-stage diversification. This scaffold integrates readily into kinase inhibitor and medicinal chemistry libraries, offering enhanced solubility and metabolic stability under standard conditions.
1-(6-Bromopyridin-3-yl)-4-methylpiperazine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions to construct biaryl and heteroaryl scaffolds. The bromopyridine moiety provides a reliable handle for C–C bond formation, while the piperazine nitrogen offers tunable basicity and hydrogen-bonding capacity. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient synthesis of complex molecular architectures in 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-H320-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: