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Structure of 53710-17-1
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2,6-Diiodopyridine serves as a highly reactive pyridine scaffold featuring two iodine substituents at the 2 and 6 positions, creating a sterically constrained, electron-deficient platform. This configuration enables selective cross-coupling transformations under palladium catalysis, facilitating efficient access to functionalized heterocycles in synthetic methodology and medicinal chemistry applications.
2,6-Diiodopyridine serves as a versatile building block in synthetic organic chemistry, enabling selective functionalization at the pyridine ring due to its orthogonal reactivity. The iodine substituents facilitate palladium-catalyzed cross-coupling reactions, including Suzuki-Miyaura and Stille couplings, with high chemoselectivity. Its bench-stable nature and compatibility with diverse reaction conditions make it valuable for constructing complex heterocyclic scaffolds and advanced intermediates in 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: