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Structure of 52522-99-3
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5-Iodo-2,4-dimethoxypyrimidine features a strategically positioned iodine atom enabling efficient cross-coupling reactions. The two methoxy groups enhance solubility and stabilize the heterocyclic core under reaction conditions. This bench-stable derivative serves as a key intermediate in the synthesis of bioactive pyrimidine-based compounds.
5-Iodo-2,4-dimethoxypyrimidine serves as a versatile building block in medicinal chemistry and cross-coupling synthesis. The iodine substituent enables reliable Suzuki, Stille, and Negishi coupling reactions, while the dimethoxy groups enhance solubility and stabilize the pyrimidine core. Its bench-stable nature and predictable reactivity make it ideal for constructing heterocyclic scaffolds and functionalized API intermediates under standard reaction conditions.
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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: