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Structure of 2164-65-0
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2-Aminopyrimidine-4-carboxylic acid features a dual functional group architecture with a nucleophilic amine and an acidic carboxylic acid, enabling versatile conjugation in medicinal chemistry. This scaffold integrates readily into bioactive molecules, particularly within kinase inhibitor frameworks and antiviral agents. The compound exhibits favorable solubility and stability under standard conditions, supporting efficient synthesis and purification workflows.
2-Aminopyrimidine-4-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of pyrimidine-based scaffolds through standard coupling and cyclization reactions. Its dual functionality—amine and carboxylic acid—facilitates modular derivatization, while its inherent stability supports straightforward purification and handling. This compound functions effectively in peptide coupling, amide formation, and heterocycle construction under routine reaction conditions.
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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: