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Structure of 951884-36-9
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5-Bromo-4-ethylpyrimidine serves as a key heterocyclic scaffold for medicinal chemistry and materials synthesis. The bromine at the 5-position enables efficient cross-coupling reactions, while the ethyl group at the 4-position imparts favorable steric and electronic properties. This compound offers enhanced stability and solubility in organic media, facilitating its integration into complex molecular architectures under standard conditions.
5-Bromo-4-ethylpyrimidine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions for the construction of biologically relevant pyrimidine scaffolds. The bromine at C5 provides a reliable site for Suzuki, Stille, and Negishi couplings, while the ethyl group at C4 enhances solubility and modulates electronic properties. Bench-stable and readily purified by distillation or flash chromatography, it functions effectively in multi-step syntheses of kinase inhibitors and nucleoside analogs.
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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: