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Structure of 2750139-24-1
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This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. The tert-butoxycarbonyl-protected azetidinyl scaffold offers enhanced stability and selective reactivity in synthetic sequences involving strained heterocycles.
(1-tert-butoxycarbonylazetidin-3-yl)boronic acid serves as a stable, bench-accessible building block for the synthesis of azetidine-containing pharmaceuticals. Its boronic acid functionality enables efficient Suzuki-Miyaura cross-coupling reactions under mild conditions, while the Boc group provides orthogonal protection and facilitates purification. The molecule exhibits good functional group tolerance and is compatible with standard peptide coupling and heterocycle-forming protocols, making it a practical reagent for medicinal chemistry and process development 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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: