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Structure of 905273-91-8
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tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isoindoline-2-carboxylate integrates a boronate handle with a sterically protected isoindoline scaffold, enabling efficient Suzuki-Miyaura coupling under mild conditions. This bench-stable reagent facilitates rapid access to functionalized isoindoline architectures in late-stage diversification workflows.
tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isoindoline-2-carboxylate serves as a stable, bench-ready boronate building block for palladium-catalyzed cross-coupling reactions. The isoindoline scaffold provides a rigid, electron-rich heterocyclic core useful in medicinal chemistry, while the diborane moiety enables efficient Suzuki-Miyaura coupling under mild conditions. Functional group tolerance and straightforward purification make it ideal for modular synthesis of complex scaffolds.
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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: