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Structure of 25151-07-9
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5-Chloro-2,4-difluoropyrimidine serves as a pivotal heterocyclic scaffold in medicinal chemistry, featuring strategically positioned halogens that enable direct functionalization via cross-coupling. The electron-deficient pyrimidine ring facilitates nucleophilic substitution, while the fluorine atoms enhance metabolic stability and membrane permeability. This compound integrates readily into bioactive molecules for kinase inhibitors and antiviral agents.
5-Chloro-2,4-difluoropyrimidine serves as a versatile building block in medicinal chemistry and agrochemical synthesis. Its electrophilic chlorine at the C5 position enables efficient Suzuki-Miyaura, Buchwald-Hartwig, and nucleophilic substitution reactions. The 2,4-difluoro substitution pattern enhances metabolic stability and modulates electronic properties, facilitating access to diverse heterocyclic scaffolds. Bench-stable and readily purified, it functions reliably in multi-step syntheses requiring high functional group tolerance.
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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: