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Structure of 5388-21-6
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2-(Methylamino)pyrimidine-5-carboxylic acid features a pyrimidine core functionalized with a methylamino group at the 2-position and a carboxylic acid at the 5-position. This bifunctional scaffold integrates electron-rich amine and polar carboxylate moieties, enabling versatile conjugation in medicinal chemistry and materials synthesis. The molecule exhibits enhanced solubility and stability under standard conditions, facilitating its use in peptide coupling and heterocyclic derivatization workflows.
2-(Methylamino)pyrimidine-5-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of pyrimidine-based heterocycles relevant to kinase inhibitors and antiviral agents. The molecule combines a readily functionalizable carboxylic acid with a methylamino-substituted pyrimidine core, offering excellent stability, compatibility with standard coupling reactions, and favorable purification profiles in synthetic workflows.
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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: