Potassium quinoline-6-trifluoroborate

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Product Information

Molecular Formula
C9H6BF3KN
Molecular Weight
235.06
Description
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.
Synonyms
Potassium 6-quinolinetrifluoroborate,Potassium trifluoro(quinolin-6-yl)borate
SMILES
[B-]C1=CC2=C(C=C1)N=C(C(=C2F)F)F.[K+]
InChI
InChI=1S/C9H3BF3N.K/c10-4-1-2-6-5(3-4)7(11)8(12)9(13)14-6/h1-3H/q-1+1
InChI Key
GGLVVWSCOKJOCW-UHFFFAOYSA-N
Melting Point
147-152 °C (decomposition)
Flash Point
Not applicable
Purity
95%
Storage
2-8°C

Safety Information

Hazards
H315 - H319 - H335
Precautionary Statement
P261 - P305 + P351 + P338

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
5
Rotatable Bond Count
0
Exact Mass
231.9947702 g/mol
Monoisotopic Mass
231.9947702 g/mol
Topological Polar Surface Area
12.9Ų
Heavy Atom Count
15
Formal Charge
0
Complexity
222
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
2
Compound Is Canonicalized
Yes
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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