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Structure of 1220423-08-4
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This boronate ester integrates a stable tetramethylboronate group with an isoindoline-1,3-dione scaffold, enabling efficient cross-coupling under mild conditions. The electron-deficient heterocycle enhances reactivity in palladium-catalyzed transformations, while the bench-stable boronate moiety simplifies handling and storage.
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoindoline-1,3-dione serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its isoindoline-1,3-dione core provides a rigid, electron-deficient scaffold valuable in medicinal chemistry and materials science. The tetramethylborolane moiety enables efficient coupling with aryl and heteroaryl halides under mild conditions, offering excellent functional group tolerance and straightforward purification.
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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-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: