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Structure of 933703-11-8
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4-Aminopyrimidine-2-carboxylic acid features a dual functional group architecture: an electron-rich amino group and a carboxylic acid moiety positioned at opposing ring vertices. This arrangement enables versatile conjugation in medicinal chemistry, particularly in kinase inhibitor scaffolds and bioactive heterocycles. The compound exhibits enhanced solubility and stability under standard conditions, facilitating integration into multi-step synthesis workflows.
4-Aminopyrimidine-2-carboxylic acid serves as a versatile scaffold for constructing bioactive heterocycles, enabling efficient derivatization via amide coupling, alkylation, and metal-catalyzed cross-coupling reactions. Its dual functionality—amine and carboxylic acid—facilitates orthogonal transformations, supporting modular synthesis of pharmaceutical intermediates. The compound exhibits good bench stability and compatibility with standard purification techniques, making it well-suited for iterative synthetic workflows in medicinal chemistry and process development.
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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: