Product Name:potassium trifluoro(quinolin-7-yl)borate

IUPAC Name:potassium trifluoro(quinolin-7-yl)boranuide

CAS:1411985-64-2
Molecular Formula:C9H6BF3KN
Purity:95%
Catalog Number:CM127339
Molecular Weight:235.06

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CM127339-1g 3-4 Weeks ȀƏș

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Product Details

CAS NO:1411985-64-2
Molecular Formula:C9H6BF3KN
Melting Point:-
Smiles Code:F[B-](F)(F)C1=CC=C2C=CC=NC2=C1.[K+]
Density:
Catalog Number:CM127339
Molecular Weight:235.06
Boiling Point:
MDL No:MFCD09993444
Storage:

Category Infos

Quinolines
Quinolines are an important class of biologically active heterocyclic compounds, and their derivatives usually exhibit a variety of biological activities. They can be used as antimalarial drugs and in the preparation of other antimalarial drugs. Other important activities of quinoline derivatives include inhibitory activity against EGFR-TK and antipsychotic activity. Futhermore, quinoline scaffolds are present in various drug molecules, including the antimalarial drugs aablaquine, chloroquine, mefloquine and primaquine, and the antibacterial agents gatifloxacin, levofloxacin, and moxifloxacin.
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Borates
Borates are classified as critical materials, they are the main source of boron and have a variety of industrial applications. Organic trifluoroborate is stable to heat, air and humidity, and is a very convenient crystalline boric acid compound. Since it has a tetra-coordinated boronic acid structure after the substitution of fluorine, it does not exhibit Lewis acidity and is stable to oxidation conditions. In addition, it can be regarded as the protector of boronic acid and boronic acid ester, which can be converted into each other. The compound can generally exist stably in organic solvents, but will decompose in protic solvents to liberate trivalent boron, so it can be directly used as a substrate for Suzuki coupling. The difference between trifluoroborate and boric acid is that it must exist in a monomeric form, so the equivalent weight can be closely controlled.

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