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Structure of 2434-56-2
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4,6-Diaminopyrimidine serves as a key nitrogen-rich heterocyclic scaffold in medicinal chemistry and materials science. This bench-stable compound features two strategically positioned amino groups that enable direct functionalization, facilitating the synthesis of kinase inhibitors, antiviral agents, and advanced organic semiconductors through straightforward coupling reactions.
4,6-Diaminopyrimidine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to pyrimidine-based scaffolds. Its two amino groups facilitate sequential functionalization, orthogonally compatible with standard coupling and protection strategies. The compound exhibits good bench stability, ease of purification, and broad compatibility in amide bond formation, Suzuki-Miyaura cross-coupling, and heterocycle elaboration—making it a reliable core for developing bioactive molecules.
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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: