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Structure of 1314538-55-0
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Potassium (((tert-butoxycarbonyl)amino)methyl)trifluoroborate delivers a stable, bench-ready source of the (Boc-amino)methyl group. This trifluoroborate ester enables efficient boron-based coupling reactions in peptide synthesis and chemical biology. The Boc-protected amine and trifluoroborate handle combine to offer enhanced stability and compatibility under standard reaction conditions.
Potassium (((tert-butoxycarbonyl)amino)methyl)trifluoroborate serves as a stable, bench-friendly boron source for the synthesis of aminoalkylated heterocycles and peptide building blocks. It facilitates efficient Suzuki-Miyaura coupling reactions under mild conditions, enabling C–C bond formation with aryl and vinyl halides. The Boc-protected amine functionality offers orthogonal reactivity and simplifies purification, making it ideal for iterative synthesis in 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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362+P364
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Lot numbers can be found on the outside label of a product: