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Structure of 4983-28-2
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2-Chloro-5-hydroxypyrimidine features a reactive chlorine atom at the 2-position paired with a hydroxyl group at the 5-position, enabling selective functionalization. This bifunctional scaffold integrates readily into pharmaceutical intermediates and bioactive heterocycles under mild conditions. The compound exhibits stability under standard bench handling, facilitating its use in multi-step syntheses.
2-Chloro-5-hydroxypyrimidine serves as a versatile building block in heterocyclic synthesis, enabling regioselective functionalization at the C5 position via nucleophilic substitution. Its hydroxyl group facilitates direct coupling or derivatization under mild conditions, while the C2 chloride supports efficient cross-coupling reactions with boronic acids and amines. The compound exhibits good bench stability and compatibility with common protecting group strategies, making it valuable for constructing pyrimidine-based scaffolds in medicinal chemistry and agrochemical research.
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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: