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Structure of 89466-59-1
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2-Chloro-4-methyl-6-(methylthio)pyrimidine features a pyrimidine core functionalized with chlorine, methyl, and methylthio groups, enabling selective reactivity in heterocyclic synthesis. This electron-deficient scaffold integrates readily into pharmaceutical intermediates and agrochemical building blocks, offering enhanced stability under standard conditions.
2-Chloro-4-methyl-6-(methylthio)pyrimidine serves as a versatile pyrimidine building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds through nucleophilic substitution. The chloro group at C2 facilitates reliable coupling with amines, thiols, and other nucleophiles under mild conditions, while the methylthio substituent enhances reactivity and provides a handle for further functionalization. Bench-stable and easily purified, it functions effectively in standard synthetic workflows for API development and library synthesis.
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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: