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Structure of 73-70-1
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2,5-Dimethylpyrimidin-4-amine features a pyrimidine core with methyl groups at the 2 and 5 positions, enhancing electron density at the 4-amino site. This configuration promotes stability and facilitates coupling reactions in synthetic applications. The compound serves as a key scaffold in medicinal chemistry, particularly for kinase inhibitors and heterocyclic catalysts.
2,5-Dimethylpyrimidin-4-amine serves as a versatile building block in medicinal chemistry, enabling the construction of pyrimidine-based scaffolds prevalent in kinase inhibitors and antiviral agents. Its methyl substituents enhance metabolic stability and modulate electronic properties, while the amine group facilitates direct functionalization or salt formation. The compound exhibits excellent bench stability, solubility in common organic solvents, and compatibility with standard coupling reactions, making it ideal for iterative synthesis campaigns and high-throughput screening libraries.
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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: