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Structure of 16018-87-4
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5-Chloro-6-methylpyrimidine-2,4(1H,3H)-dione features a chlorinated pyrimidinedione core with a methyl group at the 6-position, conferring enhanced electrophilicity and stability. This scaffold serves as a key building block in medicinal chemistry, particularly for heterocyclic scaffolds requiring precise electronic tuning and metabolic resistance.
5-Chloro-6-methylpyrimidine-2,4(1H,3H)-dione serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrimidine scaffolds. Its electrophilic chlorine and acidic enolizable protons facilitate nucleophilic substitution and condensation reactions under mild conditions. The compound exhibits good bench stability and compatibility with common functional groups, making it suitable for iterative synthesis workflows in medicinal chemistry and materials science.
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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#: 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-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: