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Structure of 98136-20-0
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5-Bromo-4,6-dichloro-2-(methylthio)pyrimidine features a highly reactive pyrimidine core functionalized with bromo, dichloro, and methylthio substituents, enabling direct coupling in cross-coupling reactions. The electron-deficient ring facilitates palladium-catalyzed transformations, while the methylthio group provides a stable yet cleavable handle for downstream derivatization. This compound serves as a key building block in medicinal chemistry and agrochemical synthesis.
5-Bromo-4,6-dichloro-2-(methylthio)pyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrimidines via palladium-catalyzed cross-coupling reactions. The bromo and chloro substituents offer orthogonal reactivity for sequential functionalization, while the methylthio group provides a stable, easily removable sulfur handle. This compound exhibits excellent bench stability and facilitates clean transformations under standard reaction conditions, making it well-suited for medicinal chemistry campaigns 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: