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Structure of 88275-88-1
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3-Bromo-2-methoxyphenol offers a strategically positioned bromine atom adjacent to a phenolic hydroxyl group, enabling direct functionalization in cross-coupling reactions. The methoxy substituent enhances electron density at the ortho position, stabilizing intermediates and improving reactivity in palladium-catalyzed transformations. This bench-stable derivative serves as a key building block for bioactive molecules and advanced synthetic intermediates.
3-Bromo-2-methoxyphenol serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted phenolic scaffolds. Its bromine atom facilitates palladium-catalyzed cross-coupling reactions, while the ortho-methoxy group provides directing capability and enhanced stability. The molecule exhibits good bench stability and is readily purified by column chromatography, making it well-suited for iterative synthetic workflows.
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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: