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Structure of 2095504-38-2
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Potassium (3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)trifluoroborate delivers a stable, bench-ready boronate handle for late-stage functionalization in synthetic and medicinal chemistry. The protected azabicyclic scaffold enables selective cross-coupling under mild conditions, combining enhanced solubility with predictable reactivity in diverse reaction environments.
Potassium (3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexan-1-yl)trifluoroborate serves as a stable, bench-ready boron building block for Suzuki-Miyaura coupling reactions. The Boc-protected azabicyclic scaffold enables efficient C–C bond formation under mild conditions, with excellent functional group tolerance and compatibility in complex molecule synthesis. Its robustness facilitates straightforward purification and integration into multi-step sequences, making it a practical reagent for constructing nitrogen-containing heterocyclic motifs in medicinal chemistry and natural product derivatization.
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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: