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Structure of 6299-87-2
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6-Hydroxypyrimidine-4-carboxylic acid features a dual functional group architecture—bearing both a hydroxyl and a carboxylic acid at distinct positions on the pyrimidine core—enabling direct conjugation in synthetic routes. This arrangement supports efficient coupling reactions, particularly in medicinal chemistry scaffolds requiring polar, hydrogen-bonding motifs. The molecule exhibits enhanced solubility in aqueous and protic solvents, facilitating handling under standard bench conditions.
6-Hydroxypyrimidine-4-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling direct functionalization at both the C4 and C6 positions. Its dual functionality facilitates efficient synthesis of substituted pyrimidines via standard coupling, amidation, and cyclization protocols. The molecule exhibits favorable bench stability and compatibility with common protecting group strategies, supporting scalable development of heterocyclic scaffolds relevant to kinase inhibitors and antiviral 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: