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Structure of 1672-50-0
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4,5-Diamino-6-hydroxypyrimidine delivers a bifunctional pyrimidine scaffold featuring two amino groups and a hydroxyl moiety at the 4,5,6-positions. This arrangement enables direct integration into nucleoside analogs and heterocyclic frameworks via straightforward coupling reactions. The compound exhibits enhanced solubility in aqueous and polar organic solvents, facilitating use in synthetic workflows requiring mild reaction conditions.
4,5-Diamino-6-hydroxypyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds through standard functional group transformations. Its ortho-diamino and hydroxyl functionalities facilitate metal-catalyzed couplings, cyclizations, and derivatization under mild conditions. The compound exhibits good bench stability and compatibility with common protecting groups, making it suitable for iterative synthesis workflows in medicinal chemistry and agrochemical development.
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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: