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Structure of 98991-09-4
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2-Iodo-3-methoxyaniline delivers a reactive iodine handle paired with an electron-donating methoxy group, enabling efficient cross-coupling transformations. This ortho-substituted aryl iodide exhibits enhanced stability and solubility in polar organic solvents, facilitating use in palladium-catalyzed reactions. The strategic positioning of the methoxy moiety modulates electronic properties for selective functionalization.
2-Iodo-3-methoxyaniline serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions due to its iodine functionality. The methoxy group provides moderate electron-donating character and enhances solubility, while the aniline scaffold offers compatibility with standard protecting group strategies. Its bench-stable crystalline form facilitates handling and purification, making it well-suited for iterative synthesis workflows in API development and heterocycle construction.
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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: