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Structure of 2789593-39-9
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Potassium (((tert-butoxycarbonyl)(methyl)amino)methyl)trifluoroborate delivers a stable, bench-ready boronate handle for late-stage functionalization. This trifluoroborate integrates readily into Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. The tert-butoxycarbonyl-protected amine moiety ensures compatibility with diverse synthetic sequences and facilitates selective deprotection. Its moisture-tolerant nature simplifies handling in standard laboratory workflows.
Potassium (((tert-butoxycarbonyl)(methyl)amino)methyl)trifluoroborate serves as a stable, bench-ready source of the Boc-methylamino methyl group, enabling efficient C–N bond formation in transition-metal-catalyzed cross-coupling reactions. Its trifluoroborate moiety enhances solubility and reaction compatibility, facilitating mild, high-yielding transformations with broad functional group tolerance. Ideal for constructing nitrogen-containing scaffolds in medicinal chemistry and peptide-based synthesis.
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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: