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Structure of 36330-90-2
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3,4-Dimethyl-2(1H)-pyridinone features a fused heterocyclic core with methyl groups at the 3 and 4 positions, enhancing electron density and steric profile. This bench-stable compound serves as a key scaffold in medicinal chemistry, enabling direct incorporation into bioactive molecules through functionalization at the pyridinone nitrogen or aromatic ring.
3,4-Dimethyl-2(1H)-pyridinone serves as a versatile heterocyclic building block in medicinal chemistry, offering a stable pyridinone core with defined regiochemistry. Its functional group tolerance enables direct derivatization via alkylation, acylation, or transition-metal-catalyzed coupling reactions. The compound exhibits excellent bench stability and facilitates efficient purification, making it well-suited for modular synthesis of bioactive scaffolds and API intermediates.
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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-P501
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Lot numbers can be found on the outside label of a product: