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Structure of 858362-82-0
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This bench-stable amine features a pyridyl nitrogen and a bromomethyl group, enabling direct functionalization in cross-coupling reactions. The para-brominated scaffold supports rapid derivatization, integrating seamlessly into synthetic pathways for bioactive molecules and advanced materials.
(2-Bromopyridin-4-yl)methanamine serves as a versatile building block for constructing pyridine-based heterocycles and pharmaceutical intermediates. Its bromo group enables palladium-catalyzed cross-coupling reactions, while the primary amine facilitates derivatization via acylation, alkylation, or condensation. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for iterative synthesis in medicinal chemistry and process development workflows.
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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: