| Identification | Back Directory | [Name]
Potassium trifluoro(quinolin-6-yl)borate | [CAS]
1411985-98-2 | [Synonyms]
Potassium 6-quinolinetrifluoroborate
Potassium quinoline-6-trifluoroborate
Potassium trifluoro(quinolin-6-yl)borate | [Molecular Formula]
C9H6BF3KN | [MDL Number]
MFCD09993442 | [MOL File]
1411985-98-2.mol | [Molecular Weight]
235.055 |
| Chemical Properties | Back Directory | [Melting point ]
147-152 °C (decomposition) | [storage temp. ]
2-8°C | [form ]
solid | [InChI]
1S/C9H6BF3N.K/c11-10(12,13)8-3-4-9-7(6-8)2-1-5-14-9;/h1-6H;/q-1;+1 | [InChIKey]
ZEVIEKZCNSGAAQ-UHFFFAOYSA-N | [SMILES]
[K+].F[B-](F)(F)c1ccc2ncccc2c1 |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
36/37/38 | [Safety Statements ]
26 | [WGK Germany ]
WGK 3 | [Storage Class]
13 - Non Combustible Solids | [Hazard Classifications]
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [Uses]
Boronic acid derivatives are typically employed in palladium-catalyzed cross coupling (Suzuki reactions), where the advantages over boronic acids are increased stability in moisture and air, and organotrifluoroborates also have a known reaction stoichiometry since they do not polymerize.
Please view our Organotrifluoroborates Technology Spotlight for more information. |
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