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Structure of 1226878-98-3
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2-Chloro-5-iodo-4-methoxypyridine features a pyridine core functionalized with chlorine, iodine, and methoxy groups at distinct positions, enabling selective cross-coupling reactions. The electron-deficient aromatic ring pairs effectively with palladium catalysts, while the methoxy group enhances solubility and stabilizes intermediates under standard conditions. This compound serves as a key building block in the synthesis of advanced pharmaceuticals and agrochemicals.
2-Chloro-5-iodo-4-methoxypyridine serves as a versatile building block in cross-coupling chemistry, enabling efficient construction of substituted pyridine scaffolds. The chloro and iodo groups provide orthogonal reactivity for Pd-catalyzed coupling reactions, while the methoxy group offers moderate electron-donating character and stability under standard reaction conditions. Its bench-stable nature and compatibility with diverse functional groups facilitate reliable use in medicinal chemistry and process development workflows.
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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: