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Structure of 1780-36-5
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2,4,6-Trichloro-5-methylpyrimidine features a highly reactive pyrimidine core flanked by three chlorine atoms and a methyl group, enabling selective substitution under mild conditions. This electron-deficient heterocycle integrates efficiently into pharmaceutical intermediates and agrochemical scaffolds, offering enhanced stability during functionalization workflows.
2,4,6-Trichloro-5-methylpyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient introduction of multiple electrophilic sites for nucleophilic substitution reactions. Its electron-deficient pyrimidine core facilitates regioselective functionalization, while the methyl group enhances stability and modulates reactivity. The compound exhibits excellent bench stability and is readily purified by recrystallization, making it well-suited for use in multi-step synthesis of heterocyclic scaffolds and API intermediates.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: