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Structure of 1197957-18-8
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2-Chloro-4-iodo-5-methylpyridine features a trifunctional pyridine core with complementary halogen handles enabling sequential cross-coupling. The chlorine and iodine substituents facilitate orthogonal Pd-catalyzed transformations, while the methyl group enhances solubility and modulates electronic properties. This scaffold supports efficient diversification in medicinal chemistry and materials synthesis.
2-Chloro-4-iodo-5-methylpyridine serves as a versatile building block in cross-coupling chemistry, enabling the construction of complex heterocyclic scaffolds. The orthogonal reactivity of chlorine and iodine allows sequential functionalization under distinct catalytic conditions. Its bench-stable nature and tolerance to diverse reaction environments facilitate efficient synthesis of pharmaceutical intermediates and agrochemical candidates.
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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: