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Structure of 1430219-73-0
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Potassium (1-(tert-butoxycarbonyl)azetidin-3-yl)trifluoroborate delivers a protected azetidine trifluoroborate handle for Suzuki-Miyaura coupling. This bench-stable reagent integrates readily into complex molecular architectures, enabling efficient C–C bond formation under mild conditions. The tert-butoxycarbonyl group provides orthogonal protection, facilitating sequential functionalization in synthetic sequences.
Potassium (1-(tert-butoxycarbonyl)azetidin-3-yl)trifluoroborate serves as a stable, bench-ready boronate building block for the construction of azetidine-containing scaffolds in medicinal chemistry. It enables palladium-catalyzed cross-coupling reactions with aryl and vinyl halides under mild conditions, offering high functional group tolerance and predictable stereochemical integrity. The Boc-protected amine functionality allows for orthogonal derivatization, facilitating downstream synthesis of bioactive molecules.
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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: