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Structure of 21901-41-7
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4-Methyl-5-nitropyridin-2(1H)-one features a fused heterocyclic core with a methyl group at the 4-position and a nitro substituent at the 5-position, delivering enhanced electron-withdrawing character. This configuration supports stable integration into pharmaceutical intermediates and functional materials, offering improved reactivity in nucleophilic substitution and coupling processes under standard conditions.
4-Methyl-5-nitropyridin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling the construction of nitrogen-containing heterocycles via standard functional group manipulations. The nitro group facilitates reduction to an amine for downstream coupling or cyclization, while the pyridinone core provides a stable scaffold with moderate polarity, aiding purification and crystallization. Bench-stable and compatible with common reaction conditions, it functions effectively in multistep synthesis workflows requiring regioselective transformations.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352
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Lot numbers can be found on the outside label of a product: