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Structure of 1004-75-7
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2,5,6-Triaminopyrimidin-4(3H)-one features a triamine-substituted pyrimidinone core with enhanced solubility and stability under physiological conditions. This scaffold integrates readily into bioactive molecule design, offering multiple amine handles for conjugation and hydrogen bonding capacity. Its electron-rich nature supports interactions in enzyme inhibition and nucleic acid targeting applications.
2,5,6-Triaminopyrimidin-4(3H)-one serves as a versatile scaffold for heterocyclic synthesis, enabling the construction of purine analogs and bioactive molecules through established amine functionalization and cyclization pathways. Its three amino groups provide orthogonal reactivity for selective derivatization, while the enolizable carbonyl supports metal coordination and hydrogen bonding in medicinal chemistry applications. The compound exhibits bench stability and facilitates straightforward purification, making it well-suited for use in iterative synthesis workflows targeting kinase inhibitors and nucleoside derivatives.
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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: