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Structure of 13924-99-7
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6-Oxo-1,6-dihydropyrazine-2-carboxylic acid features a fused heterocyclic core with a ketone at the 6-position and a carboxylic acid at C2, enabling direct incorporation into peptide mimetics and bioactive scaffolds. The electron-deficient pyrazine ring facilitates nucleophilic addition and transition-metal-catalyzed coupling reactions under mild conditions. This bench-stable intermediate supports efficient synthesis of pharmacologically relevant compounds in medicinal chemistry workflows.
6-Oxo-1,6-dihydropyrazine-2-carboxylic acid serves as a versatile building block in the synthesis of pyrazine-based heterocycles and bioactive molecules. Its conjugated enone-carboxylic acid motif enables facile functionalization via nucleophilic addition, decarboxylation, or transition-metal-catalyzed coupling. The molecule exhibits good bench stability and compatibility with common protecting group strategies, facilitating its use in medicinal chemistry campaigns targeting kinase inhibitors and antimicrobial agents.
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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: