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Structure of 34171-40-9
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2,4-Dichloro-5-ethylpyrimidine serves as a pivotal electrophilic scaffold in heterocyclic synthesis, featuring reactive chlorine sites at C2 and C4 that enable selective functionalization. The ethyl substituent at C5 enhances solubility and modulates electronic properties, while the pyrimidine core provides a robust platform for coupling reactions under mild conditions. This compound demonstrates excellent stability and compatibility with diverse reaction environments.
2,4-Dichloro-5-ethylpyrimidine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of pyrimidine-based scaffolds. The dichloro substitution pattern facilitates nucleophilic aromatic substitution reactions at C2 or C4, while the ethyl group at C5 provides steric and electronic modulation. Its bench-stable nature and compatibility with diverse coupling partners make it well-suited for iterative functionalization in API development workflows.
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: