cas 936329-97-4|| where to buy Potassium ((4-(tert-butoxycarbonyl)piperazin-1-yl)methyl)trifluoroborate

Nombre del producto:Potassium ((4-(tert-butoxycarbonyl)piperazin-1-yl)methyl)trifluoroborate

IUPAC Name:potassium ({4-[(tert-butoxy)carbonyl]piperazin-1-yl}methyl)trifluoroboranuide

: CAS：936329-97-4; Fórmula molecular：C10H19BF3KN2O2; Pureza：95%

: Número de catálogo：CM169932; Peso molecular：306.18

Unidad de embalaje	Stock disponible	Precio($)
CM169932-5g	in stock	ȀȀň
CM169932-25g	in stock	ňǯƻ

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Detalles del producto

: Núm. De CAS :936329-97-4; Fórmula molecular:C10H19BF3KN2O2; Punto de fusión:-; Código de sonrisas:F[B-](F)(CN1CCN(C(OC(C)(C)C)=O)CC1)F.[K+]; Densidad:

: Número de catálogo:CM169932; Peso molecular:306.18; Punto de ebullición:; Nº Mdl:MFCD10566514; Almacenamiento:Store at 2-8°C.

Category Infos

: Piperazines; Piperazine is an organic compound consisting of a six-membered ring containing two nitrogen atoms in opposite positions in the ring. The chemical formula of piperazine is C4H10N2, and it is an important pharmaceutical intermediate. Pyrimidines and piperazines are known to be the backbone of many bulk compounds and important core structures for approved drugs; studies have shown that combining a pyridine ring with a piperazine moiety within a single structural framework enhances biological activity.

: 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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