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Structure of 35691-20-4
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2-Chloro-4-(pyrrolidin-1-yl)pyrimidine features a pyrrolidinyl group that enhances solubility and reactivity, enabling efficient coupling in late-stage functionalization. The chlorine atom serves as a potent electrophilic handle for palladium-catalyzed cross-coupling, facilitating rapid access to complex heterocycles. This bench-stable scaffold integrates seamlessly into medicinal chemistry libraries.
2-Chloro-4-(pyrrolidin-1-yl)pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of kinase inhibitor scaffolds. The chloropyrimidine moiety facilitates nucleophilic substitution with amines, alcohols, and thiols under mild conditions, while the pyrrolidinyl group enhances solubility and modulates electronic properties. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for parallel synthesis and lead optimization campaigns.
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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: