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Structure of 308348-93-8
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Methyl 2-aminopyrimidine-5-carboxylate features a pyrimidine core bearing an amino group at C2 and a methyl ester at C5, enabling direct incorporation into heterocyclic scaffolds. The electron-rich amine facilitates nucleophilic coupling reactions, while the ester group supports selective derivatization under mild conditions. This compound serves as a key intermediate in medicinal chemistry for constructing kinase inhibitors and antiviral agents.
Methyl 2-aminopyrimidine-5-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds. Its amino and ester functionalities offer orthogonal reactivity for late-stage diversification via coupling, amidation, or cyclization reactions. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis campaigns targeting 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: