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Structure of 767-15-7
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2-Amino-4,6-dimethylpyrimidine features a pyrimidine core with amino and methyl substituents enabling versatile integration into pharmaceutical scaffolds. The para-amino group enhances nucleophilicity, while the symmetric dimethyl substitution provides steric shielding and improved metabolic stability. This compound serves as a key building block in heterocyclic synthesis, particularly for kinase inhibitors and antiviral agents.
2-Amino-4,6-dimethylpyrimidine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to pyrimidine-based scaffolds. Its well-defined reactivity supports direct functionalization at the amino and methyl positions, facilitating C–N and C–C coupling reactions under standard conditions. The compound exhibits excellent bench stability and ease of purification, making it ideal for use in multi-step syntheses and high-throughput screening campaigns.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: