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Structure of 89694-44-0
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This boronate moiety features a methoxy group at the 5-position and bromine at the 2-position, enabling selective cross-coupling in Suzuki-Miyaura reactions. The para-substitution pattern enhances stability and facilitates efficient functionalization under standard conditions.
2-Bromo-5-methoxybenzene boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient C–C bond formation under standard Suzuki-Miyaura conditions. The methoxy group provides electronic modulation and enhances solubility, while the boronic acid functionality offers excellent stability and compatibility with diverse functional groups. Its bench-stable nature and predictable reactivity make it ideal for constructing substituted aryl scaffolds in medicinal chemistry and materials science applications.
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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: