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Structure of 870718-04-0
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This boronic acid features a strategically positioned bromo group and isopropoxy substituent, enabling selective cross-coupling reactions. The electron-deficient aryl moiety enhances reactivity in Suzuki-Miyaura transformations, while the bench-stable boronate facilitates handling under standard conditions.
(3-Bromo-2-isopropoxyphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. The boronic acid functionality exhibits excellent bench stability and tolerates a range of functional groups, while the bromo substituent provides orthogonal reactivity for further diversification. Its isopropoxy group enhances solubility and reduces protodeboronation, facilitating purification and scalability in 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: