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Structure of 22433-68-7
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4-Amino-5-methylpyrimidine serves as a key heterocyclic scaffold in medicinal chemistry, offering a polar amine group and a methyl substituent that enhance solubility and metabolic stability. This pyrimidine derivative integrates readily into kinase inhibitors and nucleoside analogs, where its electron-rich core supports hydrogen bonding and targeted receptor engagement under standard bench conditions.
4-Amino-5-methylpyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds prevalent in kinase inhibitors and antiviral agents. Its amino and methyl groups offer orthogonal functionalization sites, supporting diverse derivatization via coupling, alkylation, or transition-metal-catalyzed transformations. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for high-throughput synthesis and process-scale applications.
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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: