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Structure of 1438382-15-0
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3-(Aminomethyl)-4-methoxy-6-methylpyridin-2(1H)-one features a pyridinone core functionalized with a methoxy group at C4, a methyl substituent at C6, and a strategically positioned aminomethyl side chain. This combination imparts enhanced solubility and metabolic stability, enabling efficient incorporation into bioactive scaffolds. The molecule serves as a key building block for targeted kinase inhibitors and medicinal chemistry campaigns requiring nitrogen-rich heterocycles with tunable polarity.
3-(Aminomethyl)-4-methoxy-6-methylpyridin-2(1H)-one serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to pyridone-based scaffolds. Its aminomethyl group facilitates downstream functionalization via alkylation or reductive amination, while the methoxy and methyl substituents enhance solubility and metabolic stability. The compound exhibits bench stability and compatibility with standard coupling protocols, making it suitable for parallel synthesis campaigns and API intermediate 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: