Produktname:Potassium (4-cbz-aminophenyl)trifluoroborate

IUPAC Name:potassium (4-{[(benzyloxy)carbonyl]amino}phenyl)trifluoroboranuide

CAS:850623-45-9
Molekulare Formel:C14H12BF3KNO2
Reinheit:95%
Katalognummer:CM217373
Molekulargewicht:333.16

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Produkt-Details

CAS-Nr.:850623-45-9
Molekulare Formel:C14H12BF3KNO2
Schmelzpunkt:-
SMILES-Code:F[B-](F)(C1=CC=C(NC(OCC2=CC=CC=C2)=O)C=C1)F.[K+]
Dichte:
Katalognummer:CM217373
Molekulargewicht:333.16
Siedepunkt:
Mdl-Nr.:MFCD04115743
Lagerung:Store at 2-8°C.

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.
Benzenes
Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.

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Product Other Information

Product Overview Potassium (4-cbz-aminophenyl)trifluoroborate (K-APTFB) is a trifluoroborate salt of an aminophenyl derivative of 4-chlorobenzaldehyde, an organic compound with a wide range of applications in scientific research. K-APTFB is a highly water-soluble, non-toxic, and stable compound, making it an ideal choice for a variety of laboratory experiments. It is used in organic synthesis, as a catalyst, and as a reagent in various biochemical and physiological reactions. K-APTFB has been extensively studied for its potential applications in the field of medicinal chemistry and drug design.
Synthesis and Application Potassium (4-cbz-aminophenyl)trifluoroborate is synthesized by reacting 4-chlorobenzaldehyde with potassium trifluoroborate in an aqueous solution. The reaction is conducted at room temperature and is catalyzed by an acid, such as hydrochloric acid, to produce the desired product. The reaction is fast and efficient, and yields a high purity product. Potassium (4-cbz-aminophenyl)trifluoroborate has a wide range of applications in scientific research. It is used as a reagent in organic synthesis, as a catalyst in various biochemical and physiological reactions, and as a tool for drug design and medicinal chemistry. It is also used in the synthesis of various organic compounds, such as peptides, nucleotides, and other biologically active molecules. Potassium (4-cbz-aminophenyl)trifluoroborate is also used in the synthesis of organic compounds for use in drug delivery systems.
Future Directions Potassium (4-cbz-aminophenyl)trifluoroborate has potential applications in a wide range of fields, including drug design and medicinal chemistry, organic synthesis, and biochemical and physiological research. Future research should focus on exploring the potential of Potassium (4-cbz-aminophenyl)trifluoroborate in these areas, as well as further investigating its mechanism of action and its biochemical and physiological effects. Additionally, further research should be conducted to investigate the use of Potassium (4-cbz-aminophenyl)trifluoroborate in the synthesis of organic compounds for use in drug delivery systems.