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Structure of 280582-25-4
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2,4-Dichloro-5-ethoxypyrimidine features a pyrimidine core bearing two chlorine substituents and a terminal ethoxy group, enabling selective coupling reactions in medicinal chemistry. This electron-deficient heterocycle serves as a key intermediate for synthesizing kinase inhibitors and antiviral agents, offering high reactivity under mild conditions with excellent functional group tolerance.
2,4-Dichloro-5-ethoxypyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient construction of pyrimidine-based scaffolds. Its dual chloro substituents facilitate nucleophilic substitution reactions under mild conditions, while the ethoxy group enhances solubility and stability. This compound functions effectively in Pd-catalyzed cross-coupling and amination processes, offering reliable access to substituted pyrimidines relevant to agrochemical and medicinal chemistry applications.
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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: