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Structure of 865156-50-9
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(4-Bromopyridin-2-yl)methanamine features a pyridine ring bearing both bromo and amino-methyl substituents at meta positions, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. The electron-deficient pyridine ring enhances reactivity toward palladium-catalyzed transformations, while the primary amine group provides a handle for derivatization. This bifunctional scaffold supports efficient access to bioactive heterocycles and advanced intermediates in medicinal chemistry.
(4-Bromopyridin-2-yl)methanamine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based scaffolds through palladium-catalyzed cross-coupling reactions. The bromine and primary amine functionalities offer orthogonal reactivity for sequential derivatization, while the compound exhibits good bench stability and ease of purification. Functions effectively in Suzuki, Sonogashira, and Buchwald-Hartwig coupling protocols, facilitating rapid access to diverse heterocyclic architectures relevant to drug discovery programs.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3265
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Class : 8
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Packing Group : Ⅲ
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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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