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Structure of 56686-16-9
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5-Bromo-2,4-dimethoxypyrimidine serves as a key heterocyclic building block in medicinal chemistry and agrochemical synthesis. The electron-deficient pyrimidine core facilitates nucleophilic substitution, while the bromine at C5 enables efficient coupling reactions. The dimethoxy groups enhance solubility and direct regioselective functionalization under standard conditions.
5-Bromo-2,4-dimethoxypyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds through palladium-catalyzed cross-coupling reactions. The bromine moiety provides high reactivity in Suzuki, Stille, and Negishi couplings, while the dimethoxy groups enhance solubility and offer orthogonal protection for downstream functionalization. This compound exhibits excellent bench stability and is readily purified by flash chromatography or recrystallization, making it ideal for use in medicinal chemistry and process development 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: