cas 143314-16-3|| where to buy 1-Ethyl-3-methyl-1H-imidazol-3-ium tetrafluoroborate

Nombre del producto:1-Ethyl-3-methyl-1H-imidazol-3-ium tetrafluoroborate

IUPAC Name:1-ethyl-3-methyl-1H-imidazol-3-ium; tetrafluoroboranuide

Unidad de embalaje	Stock disponible	Precio($)
CM187486-100g	in stock	ƋƱ
CM187486-500g	in stock	Ʊƙȷ

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: Núm. De CAS :143314-16-3; Fórmula molecular:C6H11BF4N2; Punto de fusión:-; Código de sonrisas:C[N+]1=CN(CC)C=C1.F[B-](F)(F)F; Densidad:

: Número de catálogo:CM187486; Peso molecular:197.97; Punto de ebullición:; Nº Mdl:MFCD00216668; Almacenamiento:Store at room temperature.

: Imidazoles; Imidazole is an important five-membered nitrogen-containing heterocyclic compound. Among the numerous heterocyclic compounds, imidazole and its derivatives are regarded as a unique and multifaceted scaffold material due to their diverse applications in industrial, organic and pharmaceutical chemistry. Imidazoles interact in different ways with many therapeutic targets, enzymes and receptors in biological systems and thus exhibit a wide range of biological activities. In particular, several imidazoles can be used as clinical drugs to treat various types of cancer with high therapeutic efficacy. Furthermore, imidazoles are one of the most critical segments in the field of anti-covid-19 virus drug discovery due to their ability to interact with active targets in living systems.; Imidazole Manufacturer; As a professional imidazole manufacturer, we can guarantee product quality and delivery time.our company has been committed to supply personalized product solutions to customers,pls consult us.

: 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.