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Structure of 905306-69-6
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2-Aminomethyl-5-methoxypyridine features a pyridine core functionalized with a methoxy group at the 5-position and a primary amine-bearing methyl linker at the 2-position. This configuration enables direct integration into bioactive scaffolds, offering enhanced solubility and metabolic stability in medicinal chemistry applications. The pendant amine facilitates conjugation or salt formation for improved formulation properties.
2-Aminomethyl-5-methoxypyridine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based scaffolds through standard functional group transformations. Its amine and methoxy groups offer orthogonal reactivity, facilitating derivatization via alkylation, acylation, or coupling reactions. The compound exhibits good bench stability and is readily purified by standard chromatographic methods, making it well-suited for iterative synthesis workflows in API development.
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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: