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Structure of 94838-82-1
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This boronate ester features a benzo[d][1,3]dioxol-5-yl moiety integrated with a tetramethyl-substituted dioxaborolane ring, delivering enhanced stability and reactivity in cross-coupling processes. The electron-rich aromatic system pairs with the bench-stable boronate functionality, enabling efficient Suzuki-Miyaura coupling under mild conditions.
2-(Benzo[d][1,3]dioxol-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. Its 1,3-dioxaborolane moiety exhibits excellent functional group tolerance and compatibility with diverse aryl and heteroaryl electrophiles. The benzo[d][1,3]dioxol-5-yl group provides a rigid, electron-rich scaffold useful in constructing bioactive heterocycles and pharmaceutical intermediates.
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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: