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Structure of 873-83-6
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4-Amino-2,6-dihydroxypyrimidine serves as a key heterocyclic scaffold in medicinal chemistry, featuring orthogonal hydroxyl and amino groups that enable selective derivatization. This electron-rich pyrimidine core supports robust hydrogen bonding and integrates readily into nucleoside analogs and kinase inhibitors. The compound demonstrates stability under standard bench conditions and facilitates efficient coupling reactions in synthetic pathways.
4-Amino-2,6-dihydroxypyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds through standard functionalization protocols. Its ortho-diol and amino functionalities offer high reactivity in coupling and condensation reactions, facilitating the construction of medicinally relevant frameworks. The compound exhibits good bench stability and is readily purified by recrystallization, supporting its use in scalable synthetic workflows.
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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: