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Merck
CN

761214

Sigma-Aldrich

Potassium quinoline-6-trifluoroborate

95%

Synonym(s):

Potassium 6-quinolinetrifluoroborate, Potassium trifluoro(quinolin-6-yl)borate

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About This Item

Empirical Formula (Hill Notation):
C9H6BF3KN
Molecular Weight:
235.06
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
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Assay

95%

form

solid

mp

147-152 °C (decomposition)
308-313 °C

storage temp.

2-8°C

SMILES string

[K+].F[B-](F)(F)c1ccc2ncccc2c1

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

InChI key

ZEVIEKZCNSGAAQ-UHFFFAOYSA-N

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Application

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.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

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

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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