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Structure of 27192-21-8
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5-Bromo-4-chloro-6-cyclopropylpyrimidine features a sterically hindered cyclopropyl group and dual halogen substituents that enable selective cross-coupling reactions under mild conditions. This electron-deficient pyrimidine scaffold serves as a key building block in the synthesis of functionalized heterocycles for medicinal chemistry applications.
5-Bromo-4-chloro-6-cyclopropylpyrimidine serves as a versatile building block for constructing substituted pyrimidines via cross-coupling and nucleophilic substitution reactions. The orthogonal halogen functionality enables sequential functionalization, while the cyclopropyl group enhances metabolic stability and modulates electronic properties. Its bench-stable nature and compatibility with Pd-catalyzed coupling protocols facilitate efficient synthesis of advanced heterocyclic scaffolds relevant to medicinal chemistry and agrochemical development.
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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 : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: