All Photos(2)

659274

Sigma-Aldrich

Potassium allyltrifluoroborate

95%

Synonym(s):
Potassium trifluoro(prop-2-enyl)borate
Empirical Formula (Hill Notation):
C3H5BF3K
CAS Number:
Molecular Weight:
147.98
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

95%

mp

>300 °C

SMILES string

[K+].F[B-](F)(F)CC=C

InChI

1S/C3H5BF3.K/c1-2-3-4(5,6)7;/h2H,1,3H2;/q-1;+1

InChI key

TVPZAMJXLCDMIT-UHFFFAOYSA-N

Application

Organotrifluoroborate involved in:
  • Catalytic allylboration
  • Stereoselective nucleophilic addition
  • Pd-catalyzed heterocyclizations
  • Oxidation reactions and Oxidative Mannich reactions
  • Cross-coupling reactions

Organotrifluoroborates as versatile and stable boronic acid surrogates.

Packaging

1 g in poly bottle

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK Germany

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

Certificate of Analysis

Certificate of Origin

Articles

Potassium Organotrifluoroborates

These bench stable Potassium Organotrifluoroborates are useful for Suzuki-Miyaura cross-coupling reactions and have also been used for a variety of other C-C bond forming reactions. Importantly, these reagents are compatible with a wide range of functional groups and are stable to many commonly used and harsh reaction conditions.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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