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Structure of 2259853-06-8
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2,6-Bis(benzyloxy)-3-iodopyridine features a pyridine core functionalized with two benzyloxy groups at the 2 and 6 positions and an iodine atom at the 3 position. This configuration enables efficient cross-coupling reactions in late-stage diversification, particularly in Suzuki-Miyaura and Negishi protocols. The benzyloxy substituents provide steric protection and enhance solubility, while the iodide serves as a high-reactivity handle for transition-metal-catalyzed transformations. The molecule exhibits excellent bench stability under standard conditions.
2,6-Bis(benzyloxy)-3-iodopyridine serves as a versatile building block for late-stage functionalization in medicinal chemistry and heterocyclic synthesis. The iodine moiety enables palladium-catalyzed cross-coupling reactions with broad functional group tolerance, while the ortho-benzyloxy groups provide steric protection and enhanced solubility. This compound exhibits excellent bench stability and facilitates efficient purification, making it well-suited for iterative synthetic sequences and API intermediate 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: