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Structure of 1430219-72-9
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This potassium {1-[(tert-butoxy)carbonyl]pyrrolidin-3-yl}trifluoroborate delivers a stable, bench-ready boronate handle for late-stage functionalization. The tert-butyl carbamate-protected pyrrolidine scaffold enhances solubility and stability, enabling efficient cross-coupling under mild conditions. This reagent integrates seamlessly into synthetic workflows requiring selective C–C bond formation.
Potassium {1-[(tert-butoxy)carbonyl]pyrrolidin-3-yl}trifluoroborate serves as a stable, bench-ready source of the pyrrolidin-3-yl trifluoroborate moiety, enabling efficient Suzuki-Miyaura cross-coupling reactions. Its tert-butyl carbamate protection ensures compatibility with diverse reaction conditions and facilitates downstream deprotection for amine functionalization. The reagent exhibits excellent functional group tolerance and simplifies purification in complex molecule 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: