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Structure of 39889-94-6
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5-Amino-2-methylpyrimidine serves as a key heterocyclic scaffold in medicinal chemistry, offering a tunable platform for bioactive compound synthesis. The amino and methyl groups enable strategic functionalization, while the pyrimidine core provides metabolic stability and favorable pharmacokinetic properties in drug discovery applications.
5-Amino-2-methylpyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. Its amino and methyl groups provide orthogonal functional handles for selective derivatization, including amidation, alkylation, and transition-metal-catalyzed coupling 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: