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Structure of 550347-54-1
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2-Chloro-5-iodo-4-methylpyridine features a trifunctional pyridine core with complementary halogen handles enabling sequential cross-coupling. The chlorine and iodine positions facilitate palladium-catalyzed transformations under standard conditions, while the methyl group provides steric and electronic modulation. This molecule serves as a key scaffold for constructing complex heterocyclic architectures in medicinal chemistry and materials science.
2-Chloro-5-iodo-4-methylpyridine serves as a versatile building block in medicinal chemistry and catalytic cross-coupling reactions. The ortho-chloro and meta-iodo substituents enable sequential functionalization via palladium-catalyzed couplings, while the methyl group provides steric and electronic modulation. Bench-stable and compatible with standard reaction conditions, it facilitates efficient access to substituted pyridine scaffolds prevalent in API development.
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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: