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Structure of 1072438-54-0
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Methyl 2-(aminomethyl)pyridine-4-carboxylate hydrochloride delivers a pyridyl-directed amine handle with enhanced solubility and stability. The protonated amine facilitates efficient salt formation, improving handling and compatibility in synthetic workflows. This bench-stable derivative integrates readily into medicinal chemistry campaigns requiring nitrogen-rich heterocycles.
Methyl 2-(aminomethyl)pyridine-4-carboxylate hydrochloride serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based scaffolds. The amine functionality facilitates conjugation and derivatization, while the ester group supports selective transformations. Its crystalline form ensures excellent bench stability and ease of handling, making it well-suited for iterative synthesis campaigns 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: