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Structure of 126354-30-1
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N-(5-Methyl-2-oxo-2,3-dihydropyrimidin-4-yl)benzamide features a fused dihydropyrimidinone core bearing a methyl group at C5 and a benzoyl substituent at N4. This electron-deficient scaffold integrates readily into heterocyclic synthesis, serving as a key building block for bioactive compound libraries under standard bench conditions.
N-(5-Methyl-2-oxo-2,3-dihydropyrimidin-4-yl)benzamide serves as a versatile building block in medicinal chemistry, enabling the construction of dihydropyrimidine-based scaffolds with demonstrated utility in kinase inhibitor and antiviral agent development. Its amide functionality offers excellent stability and compatibility with standard coupling reactions, while the 5-methyl substitution enhances metabolic resistance. The molecule facilitates efficient derivatization and purification, making it well-suited for high-throughput synthesis and scale-up applications.
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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-H320-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: