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Structure of 50593-92-5
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5-Bromo-2-(methylthio)pyrimidine-4-carboxylic acid features a pyrimidine core bearing bromine, methylthio, and carboxylic acid substituents at strategic positions. This electron-deficient scaffold integrates readily into synthetic sequences requiring halogenation or sulfur-directed functionalization. The carboxylic acid group enables direct coupling or salt formation, enhancing solubility and reactivity in diverse reaction media.
5-Bromo-2-(methylthio)pyrimidine-4-carboxylic acid serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrimidines via palladium-catalyzed cross-coupling. The bromo group facilitates C–C bond formation, while the methylthio and carboxylic acid functionalities offer orthogonal reactivity for further derivatization. Its bench-stable nature and compatibility with standard purification methods make it well-suited for iterative synthesis 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: