CAS 128796-39-4

Ácido 4-(trifluorometil)fenilborónico

Descrição:

Ácido 4-(trifluorometil)fenilborónico é um composto organoboronado caracterizado pela presença de um grupo funcional ácido bórico ligado a um anel fenílico que possui um substituinte trifluorometílico. Este composto normalmente apresenta uma aparência cristalina branca a off-white e é solúvel em solventes orgânicos polares. O grupo trifluorometílico aumenta a lipofilicidade do composto e pode influenciar sua reatividade e interação com sistemas biológicos. Como um ácido bórico, pode participar de várias reações químicas, incluindo acoplamento de Suzuki, que é significativo na síntese orgânica para a formação de ligações carbono-carbono. Além disso, pode atuar como um ácido de Lewis, coordenando-se com bases e desempenhando um papel na catálise. A presença do grupo trifluorometílico também pode conferir propriedades eletrônicas únicas, tornando-o útil no desenvolvimento de produtos farmacêuticos e agroquímicos. No geral, Ácido 4-(trifluorometil)fenilborónico é um composto versátil com aplicações em química sintética e ciência dos materiais.

Fórmula: C₇H₆BF₃O₂

InChI: InChI=1S/C7H6BF3O2/c9-7(10,11)5-1-3-6(4-2-5)8(12)13/h1-4,12-13H

Chave 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

4-(Trifluoromethyl)benzeneboronic acid, 98%

CAS: 128796-39-4

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

Fórmula: C₇H₆BF₃O₂

Pureza: 98%

Cor e Forma: White to pale cream, Powder

Peso molecular: 189.93

Ref: 02-B22374

Boronic acid, B-[4-(trifluoromethyl)phenyl]-

CAS: 128796-39-4

Fórmula: C₇H₆BF₃O₂

Pureza: 98%

Cor e Forma: Solid

Peso molecular: 189.9275

Ref: IN-DA000YEL

4-(Trifluoromethyl)benzeneboronic acid

CAS: 128796-39-4

4-(Trifluoromethyl)benzeneboronic acid

Fórmula: C₇H₆BF₃O₂

Pureza: 98%

Cor e Forma: White Solid-Powder

Peso molecular: 189.92754

Ref: 54-PC1111

4-(Trifluoromethyl)phenylboronic acid

CAS: 128796-39-4

4-(Trifluoromethyl)benzeneboronic acid: N-arylating agent for imidazoles/amines, aids in microwave-assisted cross-coupling to aryl ketones.

Fórmula: C₇H₆BF₃O₂

Pureza: 98%

Cor e Forma: Solid

Peso molecular: 189.93

Ref: TM-T21356

4-Trifluoromethylphenylboronic acid

CAS: 128796-39-4

Fórmula: C₇H₆BF₃O₂

Peso molecular: 189.93

Ref: 7W-GK4806

4-(Trifluoromethyl)phenylboronic acid

CAS: 128796-39-4

Fórmula: C₇H₆BF₃O₂

Pureza: 99.0%

Cor e Forma: Solid

Peso molecular: 189.93

Ref: 10-F005207

4-(Trifluoromethyl)phenylboronic Acid (contains varying amounts of Anhydride)

CAS: 128796-39-4

Fórmula: C₇H₆BF₃O₂

Pureza: 97.0 to 111.0 %

Cor e Forma: White to Light yellow powder to crystal

Peso molecular: 189.93

Ref: 3B-T1788

4-(Trifluoromethyl)phenylboronic Acid

CAS: 128796-39-4

Fórmula: C₇H₆BF₃O₂

Cor e Forma: Neat

Ref: TR-T791030

4-(Trifluoromethyl)phenylboronic acid

CAS: 128796-39-4

(4-(Trifluoromethyl)phenyl)boronic acid

Fórmula: C₇H₆BF₃O₂

Pureza: 98%

Peso molecular: 189.93

Ref: IN-DG4475

4-(Trifluoromethyl)phenylboronic acid

CAS: 128796-39-4

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.

Fórmula: C₇H₆BF₃O₂

Pureza: Min. 95%

Peso molecular: 189.93 g/mol

Ref: 3D-FT70034