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Structure of 354824-19-4
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This bench-stable amine features a pyridyl core with a methoxy group at the 2-position and a primary amine at the 3-yl methyl substituent. The electron-donating methoxy enhances nucleophilicity, while the nitrogen-rich scaffold enables integration into heterocyclic systems. Ideal for coupling reactions in medicinal chemistry and catalyst design.
(2-Methoxypyridin-3-yl)methanamine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based scaffolds through standard amine functionalization. Its ortho-methoxy group provides enhanced solubility and modulates electronic properties, while the primary amine facilitates conjugation reactions, reductive amination, and coupling protocols. Bench-stable and readily purified by column chromatography, it functions effectively in multistep synthesis of bioactive molecules.
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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: