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Structure of 500305-98-6
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(3-Chloropyridin-2-yl)methanamine features a chlorinated pyridine core with a primary amine tethered to the 3-position, enabling direct functionalization in heterocyclic synthesis. This bench-stable, moisture-tolerant building block integrates readily into pharmaceutical intermediates and ligand frameworks through nucleophilic substitution or coupling reactions.
(3-Chloropyridin-2-yl)methanamine serves as a versatile building block for heterocyclic synthesis, enabling direct functionalization at the pyridine nitrogen and ortho-position. Its amine functionality facilitates coupling reactions, while the chlorine atom provides a site for palladium-catalyzed cross-coupling or nucleophilic substitution. The compound exhibits bench stability and compatibility with common protecting group strategies, making it well-suited for medicinal chemistry campaigns requiring modular scaffold assembly.
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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-H319
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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: