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Structure of 2254447-10-2
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Potassium ((1-(tert-butoxycarbonyl)azetidin-3-yl)methyl)trifluoroborate features a stable trifluoroborate moiety integrated into a protected azetidine scaffold, enabling direct cross-coupling without prior activation. This bench-stable reagent facilitates efficient incorporation of functionalized azetidinyl units into complex molecular architectures under standard Suzuki-Miyaura conditions.
Potassium ((1-(tert-butoxycarbonyl)azetidin-3-yl)methyl)trifluoroborate serves as a stable, bench-friendly boronate building block for Suzuki-Miyaura coupling reactions. The Boc-protected azetidine moiety enables direct incorporation into complex scaffolds with high functional group tolerance and predictable reactivity. Its trifluoroborate salt enhances solubility and stability compared to traditional boronic acids, facilitating efficient cross-coupling in diverse reaction conditions.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H290-H314
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Precautionary Statements : P234-P260-P264-P280-P301+P330+P331-P304+P340-P363-P390-P405-P406-P501
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Lot numbers can be found on the outside label of a product: