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Structure of 26163-03-1
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3-Bromo-5-chloropyridin-2-amine is a heterocyclic building block featuring bromo and chloro substituents at adjacent positions on the pyridine ring, enabling selective cross-coupling reactions. The amino group at C2 provides a site for derivatization, while the electron-deficient aromatic core enhances reactivity in palladium-catalyzed transformations. This scaffold supports efficient access to functionalized pyridines under standard conditions.
3-Bromo-5-chloropyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen functionality. The bromo group facilitates Suzuki, Stille, and Negishi couplings, while the chloro substituent offers enhanced stability under reaction conditions. The pyridin-2-amine moiety provides a readily derivatizable nitrogen for further functionalization. This compound exhibits good bench stability and is compatible with standard purification techniques, making it well-suited for iterative synthesis of complex heterocyclic scaffolds.
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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: