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Structure of 505084-55-9
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2-Chloro-5-(trifluoromethyl)-4-iodopyridine features a uniquely activated pyridine core with orthogonal halogen handles: a chloro group at C2 and an iodide at C4, flanked by a strongly electron-withdrawing trifluoromethyl substituent at C5. This combination enables selective cross-coupling transformations under mild conditions, particularly in Pd-catalyzed reactions where the iodo moiety serves as a high-reactivity partner. The molecule exhibits excellent bench stability and solubility in common organic solvents, facilitating use in iterative synthesis workflows.
2-Chloro-5-(trifluoromethyl)-4-iodopyridine serves as a versatile building block for palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heterocyclic scaffolds. The ortho-chloro and para-iodo substituents offer complementary reactivity for sequential functionalization. Its stability under standard reaction conditions and tolerance to diverse functional groups facilitate reliable synthesis of complex molecular architectures relevant to medicinal chemistry and materials science.
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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: