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Structure of 22715-27-1
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2,5-Diaminepyrimidine serves as a key nitrogen-rich heterocyclic scaffold in medicinal chemistry and materials science. This bench-stable compound features two strategically positioned primary amine groups that enable facile functionalization. The electron-donating character of the diamine moiety enhances reactivity in coupling reactions and facilitates coordination with metal ions. Its planar structure supports π-π stacking interactions, making it valuable for constructing supramolecular architectures and conjugated systems.
2,5-Diaminopyrimidine serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling the construction of pyrimidine-based scaffolds prevalent in pharmaceuticals. Its two amino groups offer orthogonal reactivity for selective functionalization, while its inherent stability facilitates handling and purification. Functions effectively in coupling reactions, metal-catalyzed transformations, and as a key intermediate in the development of 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: