CAS 128796-39-4
:Ácido 4-(trifluorometil)fenilborónico
Descripción:
Ácido 4-(trifluorometil)fenilborónico es un compuesto organoboronado caracterizado por la presencia de un grupo funcional ácido bórico unido a un anillo fenílico que tiene un sustituyente trifluorometilo. Este compuesto típicamente exhibe una apariencia cristalina blanca a blanco sucio y es soluble en disolventes orgánicos polares. El grupo trifluorometilo mejora la lipofilia del compuesto y puede influir en su reactividad e interacción con sistemas biológicos. Como un ácido bórico, puede participar en varias reacciones químicas, incluida la acilación de Suzuki, que es significativa en la síntesis orgánica para formar enlaces carbono-carbono. Además, puede actuar como un ácido de Lewis, coordinándose con bases y desempeñando un papel en la catálisis. La presencia del grupo trifluorometilo también puede conferir propiedades electrónicas únicas, haciéndolo útil en el desarrollo de productos farmacéuticos y agroquímicos. En general, Ácido 4-(trifluorometil)fenilborónico es un compuesto versátil con aplicaciones en química sintética y ciencia de materiales.
Fórmula:C7H6BF3O2
InChI:InChI=1S/C7H6BF3O2/c9-7(10,11)5-1-3-6(4-2-5)8(12)13/h1-4,12-13H
Clave InChI:InChIKey=ALMFIOZYDASRRC-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=CC=C(B(O)O)C=C1
Sinónimos:- 4-(Trifluoromethyl)Benzeneboronic Acid
- 4-(Trifluoromethyl)Phenylboronic Acid
- 4-[(Trifluoromethyl)-Phenyl]-Boronic Acid
- B-[4-(Trifluoromethyl)phenyl]boronic acid
- Boronic acid, B-[4-(trifluoromethyl)phenyl]-
- Boronic acid, [4-(trifluoromethyl)phenyl]-
- [p-(Trifluoromethyl)phenyl]boronic acid
- p-(Trifluoromethyl) phenylboronic acid
- α,α,α-Trifluoro-p-tolylboronic acid
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Encontrado 9 productos.
4-(Trifluoromethyl)benzeneboronic acid, 98%
CAS:<p>4-(Trifluoromethyl)benzeneboronic acid is used of this drug is to N-arylate imidazoles and amines with copper-exchanged fluorapatite, as well as used in microwave-promoted cross-coupling with acid chlorides leading to aryl ketones. This Thermo Scientific Chemicals brand product was originally part o</p>Fórmula:C7H6BF3O2Pureza:98%Forma y color:White to pale cream, PowderPeso molecular:189.93Boronic acid, B-[4-(trifluoromethyl)phenyl]-
CAS:Fórmula:C7H6BF3O2Pureza:98%Forma y color:SolidPeso molecular:189.9275Ref: IN-DA000YEL
1g26,00€5g30,00€10g34,00€1kgA consultar25g60,00€2kgA consultar50g85,00€5kgA consultar100g116,00€500g543,00€4-(Trifluoromethyl)phenylboronic acid
CAS:4-(Trifluoromethyl)benzeneboronic acid: N-arylating agent for imidazoles/amines, aids in microwave-assisted cross-coupling to aryl ketones.Fórmula:C7H6BF3O2Pureza:98%Forma y color:White PowderPeso molecular:189.934-(Trifluoromethyl)benzeneboronic acid
CAS:4-(Trifluoromethyl)benzeneboronic acidFórmula:C7H6BF3O2Pureza:98%Forma y color: white solidPeso molecular:189.93g/mol4-(Trifluoromethyl)phenylboronic Acid (contains varying amounts of Anhydride)
CAS:Fórmula:C7H6BF3O2Pureza:97.0 to 111.0 %Forma y color:White to Light yellow powder to crystalPeso molecular:189.934-(Trifluoromethyl)phenylboronic acid
CAS:Fórmula:C7H6BF3O2Pureza:99.0%Forma y color:SolidPeso molecular:189.934-(Trifluoromethyl)phenylboronic acid
CAS:<p>4-(Trifluoromethyl)phenylboronic acid is a boronic acid that has been used as a model system to study the cross-coupling reaction. This compound is synthetically challenging and has shown high resistance to degradation by natural compounds, such as dopamine. 4-(Trifluoromethyl)phenylboronic acid can also be used for o-glycosylation, a reversible covalent process in which an alcohol reacts with an unprotected carbohydrate. The compound has been shown to react with uridine and hydrogen bond with the carbonyl group of sugars, giving it the potential to serve as a fluorescent probe for detection of carbohydrates in urine samples or other biological fluids.</p>Fórmula:C7H6BF3O2Pureza:Min. 95%Peso molecular:189.93 g/mol









