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Potassium (2-((tert-butoxycarbonyl)amino)ethyl)trifluoroborate

  • CAS No. 926280-83-3

  • Cat. No. CS-0135382
  • Purity≥95%
  • MDL No.MFCD10698613

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

Potassium (2-((tert-butoxycarbonyl)amino)ethyl)trifluoroborate|CS-0135382

Structure of 926280-83-3

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General Information

  • CAS No. 926280-83-3
  • Cat. No. CS-0135382
  • Purity ≥95%
  • MDL No. MFCD10698613
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₁₄B₃F₃KNO₂ ₂-
  • Molecular Weight 272.72
  • Synonym(s) None
  • SMILES O=C(NC[CH2-]B([F-])([F-])([F-])=B[B+])OC(C)(C)C.[K+]

Description

Potassium (2-((tert-butoxycarbonyl)amino)ethyl)trifluoroborate delivers a stable, bench-ready boronate handle for Suzuki-Miyaura cross-coupling. The tert-butyl carbamate-protected amine enables orthogonal functionalization, while the trifluoroborate moiety ensures excellent stability and compatibility with diverse reaction conditions. This reagent streamlines access to complex nitrogen-containing scaffolds in medicinal chemistry and materials synthesis.

Application

Potassium (2-((tert-butoxycarbonyl)amino)ethyl)trifluoroborate serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. It enables efficient C–C bond formation under mild conditions, featuring excellent functional group tolerance and compatibility with common protecting groups. The Boc-protected amine functionality facilitates downstream deprotection and incorporation into peptide-like scaffolds or bioactive heterocycles, making it a practical reagent for medicinal chemistry and API intermediate 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

Quality Control

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Computational Chemistry Data

  • TPSA   38.33
  • LogP   -0.6375
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   3

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