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Structure of 38696-23-0
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5-Bromo-2-methoxy-4-methylpyrimidine features a pyrimidine core functionalized with bromo, methoxy, and methyl groups at strategic positions, enabling selective cross-coupling reactions. This electron-deficient heterocycle integrates readily into pharmaceutical intermediates and agrochemical scaffolds, offering high reactivity under palladium-catalyzed conditions. The methoxy and methyl substituents enhance solubility and stability during synthetic processing.
5-Bromo-2-methoxy-4-methylpyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient palladium-catalyzed cross-coupling reactions due to its well-defined electrophilic bromine site. The methoxy and methyl groups provide orthogonal functional handles for further derivatization, while the pyrimidine core offers excellent bench stability and compatibility with standard synthetic protocols.
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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: