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Structure of 97004-04-1
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This bench-stable amine features a chloropyridyl moiety enabling direct functionalization in cross-coupling reactions. The para-chloro substitution enhances electrophilic reactivity, while the primary amine group facilitates conjugation and coordination in catalytic systems.
(6-Chloropyridin-3-yl)methanamine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based scaffolds through standard coupling reactions. Its chloro group provides a reliable handle for palladium-catalyzed cross-coupling, while the primary amine facilitates derivatization via acylation, alkylation, or imine formation. The compound exhibits good bench stability and is compatible with common purification methods, making it well-suited for iterative synthesis campaigns in API development.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H315-H317-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P272-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: