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Structure of 15598-33-1
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4,6-Dichloro-5-fluoropyrimidin-2-amine features a highly reactive pyrimidine core with orthogonal halogen substituents enabling selective cross-coupling. The electron-deficient ring facilitates nucleophilic substitution under mild conditions, while the amino group serves as a direct handle for derivatization in medicinal chemistry and agrochemical synthesis.
4,6-Dichloro-5-fluoropyrimidin-2-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of kinase inhibitors and antiviral agents. Its electrophilic pyrimidine core undergoes facile nucleophilic substitution with amines, thiols, and heterocycles under mild conditions. The dichloro and fluoro substituents provide orthogonal reactivity for sequential functionalization, while the amine group offers a handle for further derivatization. Bench-stable and readily purified by recrystallization, it is well-suited for scale-up and high-throughput 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 : 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: