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900389 Sigma-Aldrich

Potassium 5-fluoro-2-isonicotinyltrifluoroborate

  • Empirical Formula (Hill Notation) C6H3BF4KNO

  • Molecular Weight 231.00

  •  NACRES NA.22

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Description

Application

Potassium acyltrifluroborates (KATs) are bench-, air-, and moisture-stable reagents for rapid chemoselective amide bond formations with hydroxylamines. These amide bond-forming reactions proceed under aqueous conditions without the need for coupling reagents or protecting groups. This product was introduced in collaboration with the Bode Research Group.

Packaging

1 g in glass bottle

Other Notes

Amide-Forming Ligation of Acyltrifluoroborates and Hydroxylamines in Water
Synthesis of Bifunctional Potassium Acyltrifluoroborates

Safety & Documentation

Safety Information

Symbol 
Signal word 
Danger
Hazard statements 
Target organs 
Respiratory system
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable

Documents

Certificate of Analysis (COA)

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Protocols & Articles

Articles

Jeffrey Bode Group – Professor Product Portal

From our library of Articles, Sigma-Aldrich presents Jeffrey Bode Group – Professor Product Portal
Keywords: Annulations, Asymmetric synthesis, Catalysis, Cross couplings, transformation

Peer-Reviewed Papers
15

References

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