製品名:Potassium (5-chlorothiophen-2-yl)trifluoroborate

IUPAC Name:potassium (5-chlorothiophen-2-yl)trifluoroboranuide

CAS番号:1190883-05-6
分子式:C4H2BClF3KS
純度:95%
カタログ番号:CM205651
分子量:224.47

包装単位 有効在庫 価格(USD) 数量
CM205651-5g in stock Ÿƚdž
CM205651-25g in stock ƴŸǫ

研究開発用専用.

問い合わせフォーム

   refresh    

製品詳細

CAS番号:1190883-05-6
分子式:C4H2BClF3KS
融点:-
SMILESコード:F[B-](F)(C1=CC=C(Cl)S1)F.[K+]
密度:
カタログ番号:CM205651
分子量:224.47
沸点:
MDL番号:MFCD19053176
保管方法:Store at 2-8°C.

Category Infos

Thiophenes
Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.
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.

Related Products