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Structure of 214290-49-0
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5-Bromopyrimidin-2-ol features a bromine substituent at the 5-position and a hydroxyl group at the 2-position on a pyrimidine core. This combination imparts enhanced reactivity for nucleophilic substitution and facilitates direct functionalization in heterocyclic synthesis. The compound serves as a key intermediate in medicinal chemistry and agrochemical development, offering reliable access to substituted pyrimidines under mild conditions.
5-Bromopyrimidin-2-ol serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds. Its bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the hydroxyl group offers potential for derivatization or protection. The compound exhibits good bench stability and is compatible with standard reaction conditions, making it a practical choice for constructing functionalized heterocycles in drug discovery and materials science applications.
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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: