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CS-W001157 4
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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
  • HazMat Fee +

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    Each bottle is packed as an Excepted Quantity, with a maximum of 1g for items in class 6.1 packing group I or II, and up to 25g for all other hazardous materials.

    If shipping is charged to your FedEx account, the HazMat fee will be billed directly by the courier. Otherwise, the fee will be included on your invoice. To help you avoid the HazMat fee, we can package a 5g order of a class 6.1 packing group I or II material as five separate 1g units, and a 100g order of any other dangerous good as four 25g units. This packaging adjustment will be made unless you instruct otherwise on your purchase order. Below, you will find the fee schedule from FedEx for handling hazardous materials.

    Type
    HazMat Fee
    Excepted Quantity $0.00
    FedEx Limited Quantities Ground $0.00
    Hazmat Ground shipping $50.00+
    Inaccessible (Haz class 6.1 or 9), Domestic $68.00+
    Accessible (Haz class 3, 4, 5 or 8), Domestic $158.00+
    Inaccessible (Haz class 6.1 or 9), International $108.00+
    Accessible (Haz class 3, 4, 5 or 8), International $238.00+

    An item is classified as a dangerous good if our website displays Hazardous Material (HazMat) information for it.

    There is a HazMat shipping fee for each item that qualifies as a dangerous good. Please contact our quotation team via email to confirm the details.

*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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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.

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+]

Computational Chemistry Data

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

Safety Information

Download SDS
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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