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Structure of 4068-75-1
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Methyl 2-hydroxy-5-iodobenzoate features a strategically positioned hydroxyl group and iodine atom on the aromatic ring, enabling selective functionalization in cross-coupling reactions. This ortho-hydroxy-iodo substitution pattern enhances reactivity in palladium-catalyzed transformations while maintaining bench stability under standard conditions.
Methyl 2-hydroxy-5-iodobenzoate serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient access to substituted phenolic scaffolds. The ortho-hydroxyl group provides a directing effect in palladium-catalyzed functionalizations, while the iodide moiety ensures high reactivity in Suzuki, Stille, and Negishi couplings. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for iterative synthesis of complex aromatic architectures in medicinal chemistry and materials science.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: