Nom du produit:potassium trifluoro(isoquinolin-6-yl)borate

IUPAC Name:potassium trifluoro(isoquinolin-6-yl)boranuide

CAS:1411986-46-3
Formule moléculaire:C9H6BF3KN
Pureté:95%
Numéro de catalogue:CM127340
Poids moléculaire:235.06

Unité d'emballage Stock disponible Prix($) Quantité
CM127340-1g in stock ȷDzſ

Pour une utilisation en R&D uniquement..

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Détails du produit

N° CAS:1411986-46-3
Formule moléculaire:C9H6BF3KN
Point de fusion:-
Code SMILES:F[B-](F)(F)C1=CC2=C(C=NC=C2)C=C1.[K+]
Densité:
Numéro de catalogue:CM127340
Poids moléculaire:235.06
Point d'ébullition:
N° Mdl:
Stockage:

Category Infos

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.
Isoquinolines
Compared to quinolines, isoquinolines are also prominent structural motifs present in many biologically significant natural and synthetic compounds. Some well-known isoquinoline alkaloids include the anticancer and anticonvulsant berberine, the vasodilator and antispasmodic drugs papaverine and emetine. In addition to naturally occurring isoquinolines, synthetic analogs have also shown significant biological activity.

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