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Structure of 1415574-30-9
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Methyl 5-hydroxypyrimidine-2-carboxylate features a pyrimidine core bearing both hydroxyl and ester functionalities, enabling direct integration into heterocyclic synthesis. The hydroxyl group offers a site for derivatization, while the ester facilitates selective transformations under mild conditions. This compound serves as a key intermediate in medicinal chemistry and agrochemical development, combining synthetic versatility with bench-stable handling.
Methyl 5-hydroxypyrimidine-2-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds. The hydroxyl group facilitates downstream derivatization via esterification, ether formation, or transition-metal-catalyzed coupling reactions. Its stability under standard bench conditions and compatibility with common protecting group strategies make it ideal for modular synthesis of heterocyclic APIs and functional intermediates.
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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: