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Structure of 34415-10-6
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This dihydropyrimidine derivative features a conjugated carbonyl system and a carboxylic acid group, enabling direct integration into peptide coupling workflows. The methyl substituent enhances stability, while the oxo and carboxylic functionalities provide versatile handles for downstream functionalization in medicinal chemistry applications.
2-Methyl-6-oxo-1,6-dihydropyrimidine-4-carboxylic acid serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds. Its conjugated enone system and carboxylic acid functionality support diverse transformations, including nucleophilic additions, decarboxylative couplings, and cyclizations. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for medicinal chemistry campaigns and process-scale 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-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: