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Structure of 850036-28-1
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1-Cyclopentenylboronic acid delivers a reactive, electron-rich boronate handle for cross-coupling reactions. The cyclopentenyl ring imparts conformational rigidity and enhanced stability under standard conditions. This bench-stable reagent integrates efficiently into Suzuki-Miyaura coupling workflows, enabling direct access to functionalized cyclic scaffolds with high selectivity.
1-Cyclopentenylboronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient access to functionalized cyclopentene derivatives. Its stability under ambient conditions and compatibility with common reaction protocols facilitate straightforward incorporation into complex molecular architectures. The boronic acid group reacts reliably with aryl, vinyl, and heteroaryl halides, offering a practical route to diversely substituted cyclopentene scaffolds relevant in medicinal chemistry and materials science.
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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: