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CS-W001157 4
Total: USD 88.00

Potassium (((tert-butoxycarbonyl)(methyl)amino)methyl)trifluoroborate

  • CAS No. 2789593-39-9

  • Cat. No. CS-0881129
  • Purity≥95%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

Potassium (((tert-butoxycarbonyl)(methyl)amino)methyl)trifluoroborate|CS-0881129

Structure of 2789593-39-9

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General Information

  • CAS No. 2789593-39-9
  • Cat. No. CS-0881129
  • Purity ≥95%
  • MDL No. None
  • Storage 4°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₁₄BF₃KNO₂
  • Molecular Weight 251.10
  • Synonym(s) None
  • SMILES F[B-](F)(CN(C(OC(C)(C)C)=O)C)F.[K+]

Description

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.

Application

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.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
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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Computational Chemistry Data

  • TPSA   29.54
  • LogP   -0.7561
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   2

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