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Structure of 56-05-3
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2-Amino-4,6-dichloropyrimidine serves as a key heterocyclic scaffold in medicinal chemistry, featuring two chlorine substituents at electron-deficient positions and a primary amine enabling downstream functionalization. This bench-stable compound integrates readily into kinase inhibitors, antiviral agents, and agrochemicals through nucleophilic substitution or coupling reactions under standard conditions.
2-Amino-4,6-dichloropyrimidine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of heterocyclic scaffolds via nucleophilic substitution. Its dichloro functionality facilitates sequential functionalization under mild conditions, while the amino group offers direct derivatization potential. The compound exhibits good bench stability and is readily purified by recrystallization, making it well-suited for scalable synthesis 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: