Nombre del producto:Potassium trifluoro(morpholinomethyl)borate

IUPAC Name:potassium trifluoro[(morpholin-4-yl)methyl]boranuide

CAS:936329-94-1
Fórmula molecular:C5H10BF3KNO
Pureza:95%
Número de catálogo:CM163820
Peso molecular:207.04

Unidad de embalaje Stock disponible Precio($) Cantidad
CM163820-5g in stock ŮŮǙ

Sólo para uso en I+D..

Formulario de consulta

   refresh    

Detalles del producto

Núm. De CAS :936329-94-1
Fórmula molecular:C5H10BF3KNO
Punto de fusión:-
Código de sonrisas:F[B-](F)(F)CN1CCOCC1.[K+]
Densidad:
Número de catálogo:CM163820
Peso molecular:207.04
Punto de ebullición:
Nº Mdl:MFCD10566512
Almacenamiento:Keep in inert atmosphere, store at 2-8°C.

Category Infos

Morpholines
Morpholine contains secondary amine groups and has all the typical reactive characteristics of secondary amine groups. It can react with inorganic acids to form salts, and react with organic acids to form salts or amides, which can be subjected to alkylation reaction, and can also be reacted with ethylene oxide, ketone or Willgerodt reaction. Morpholine is a six-membered ring containing oxygen and nitrogen, and its alkalinity is much lower than that of its parent piperidine. The marketed morpholine drugs are mainly distributed in the fields of tumors, cardiovascular and cerebrovascular diseases, respiratory system diseases, digestive system diseases, infectious diseases and mental disorders.
morpholine price
if you are interested in morpholine price, please feel free to contact us. More information of our products will be forwarded to you upon receipt of your specific inquiry.
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