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Structure of 49844-93-1
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2-Chloro-4-(methylthio)pyrimidine features a reactive chlorine atom at the 2-position paired with a methylthio group at the 4-position, enabling efficient coupling in heterocyclic synthesis. This electron-deficient pyrimidine scaffold integrates readily into pharmaceutical intermediates and agrochemical frameworks under mild conditions.
2-Chloro-4-(methylthio)pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. The chloro group facilitates nucleophilic substitution reactions, while the methylthio moiety offers orthogonal reactivity and stability under standard synthetic conditions. This compound functions effectively in Pd-catalyzed cross-coupling processes and supports the synthesis of biologically relevant heterocycles with high functional group tolerance and ease of purification.
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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: