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Structure of 1142197-44-1
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2-Bromo-5-(piperidin-1-yl)pyridine features a brominated pyridine core paired with a piperidinyl substituent, enabling efficient coupling in cross-coupling reactions. The electron-rich piperidine moiety enhances solubility and reactivity, while the bromine serves as a robust handle for palladium-catalyzed transformations. This compound integrates readily into complex molecular architectures under standard conditions.
2-Bromo-5-(piperidin-1-yl)pyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions to construct biaryl and heteroaryl architectures. The bromopyridine moiety offers high reactivity in Suzuki, Stille, and Negishi couplings, while the piperidinyl group provides a basic nitrogen for salt formation and potential hydrogen bonding in target molecules. Bench-stable and readily purified by column chromatography, it facilitates efficient synthesis of complex scaffolds relevant to kinase inhibitors and CNS-targeted therapeutics.
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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: