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Structure of 33630-96-5
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5-Amino-1-methylpyridin-2(1H)-one features a pyridinone core with a methyl group at C1 and an amino substituent at C5, delivering enhanced solubility and nucleophilicity. This scaffold integrates readily into heterocyclic synthesis, serving as a key building block for bioactive compounds in medicinal chemistry and materials science.
5-Amino-1-methylpyridin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through standard amine functionalization and electrophilic substitution. Its pyridone core offers enhanced solubility and hydrogen-bonding capacity, while the methyl group provides steric and electronic modulation. The compound exhibits bench stability and compatibility with common coupling reactions, facilitating efficient synthesis of kinase inhibitors and other targeted therapeutics.
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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: