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Structure of 59782-89-7
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2-Chloro-5-iodo-3-methylpyridine features a trifunctional pyridine core with orthogonal reactivity, enabling selective cross-coupling in late-stage functionalization. The chlorine and iodine substituents serve as distinct handles for Pd-catalyzed transformations, while the methyl group enhances solubility and modulates electronic properties. This scaffold supports efficient diversification in medicinal chemistry and materials synthesis under standard conditions.
2-Chloro-5-iodo-3-methylpyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The chloro group facilitates Suzuki or Negishi couplings, while the iodo substituent offers high reactivity in Stille or Sonogashira transformations. Bench-stable and compatible with common protecting groups, it supports efficient synthesis of substituted pyridine scaffolds for drug discovery 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-H312-H315-H319-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: