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Structure of 14248-01-2
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5-Bromo-1-methyl-2(1H)-pyrimidinone features a bromine substituent at the 5-position and a methyl group at the 1-position of the pyrimidinone core. This electron-deficient heterocycle serves as a key intermediate in medicinal chemistry, enabling efficient coupling reactions for nucleoside analogs and bioactive molecule synthesis under standard conditions.
5-Bromo-1-methyl-2(1H)-pyrimidinone serves as a versatile building block in heterocyclic synthesis, enabling efficient C–C and C–N bond formation via palladium-catalyzed cross-coupling reactions. Its bromine substituent provides high reactivity in Suzuki, Stille, and Negishi couplings, while the pyrimidinone core offers compatibility with diverse functional groups. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for medicinal chemistry and API intermediate development.
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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: