CAS 149104-90-5

4-Acetylphenylboronic acid

Description:

4-Acetylphenylboronic acid is an organic compound characterized by the presence of both a boronic acid functional group and an acetyl group attached to a phenyl ring. Its molecular structure features a phenyl ring substituted at the para position with an acetyl group and a boronic acid moiety, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols. It is often utilized in the development of pharmaceuticals, particularly in the synthesis of compounds that target specific biological pathways. Additionally, 4-acetylphenylboronic acid can serve as a reagent in cross-coupling reactions, which are essential in the formation of carbon-carbon bonds. Safety precautions should be observed when handling this compound, as boronic acids can be irritants and may pose environmental hazards.

Formula: C₈H₉BO₃

InChI: InChI=1/C8H9BO3/c1-6(10)7-2-4-8(5-3-7)9(11)12/h2-5,11-12H,1H3

InChI key: InChIKey=OBQRODBYVNIZJU-UHFFFAOYSA-N

SMILES: B(O)(O)C1=CC=C(C(C)=O)C=C1

Synonyms:

• 2-(Dipropan-2-Ylamino)Ethanol
• 4-Acetylbenzeneboronic acid
• 4-Boronoacetophenone
• B-(4-Acetylphenyl)boronic acid
• Boronic acid, (4-acetylphenyl)-
• Boronic acid, B-(4-acetylphenyl)-
• P-Acetylphenylboronic acid
• 4-Acetylphenylboronic acid
• TIMTEC-BB SBB000146
• 4-Acetylphenylboronic acid ,98%
• 4-Acetylphenylboronic
• RARECHEM AH PB 0162
• ACETOPHENONE-4-BORONIC ACID
• 4-ACETYLBENZENEBORONIC ACID 98+%
• AKOS BRN-0001
• 4-Acetylbenzeneboronic acid 96%
• 4-Acetylphenylboronic acid~4-Boronoacetophenone
• Boronic acid, (4-acetylphenyl)-(9CI)

4-Acetylbenzeneboronic acid, 98%

CAS: 149104-90-5

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₈H₉BO₃

Purity: 98%

Color and Shape: White to pale cream to pale yellow to pale brown, Crystals or powder or crystalline powder

Molecular weight: 163.97

Ref: 02-B23234

Boronic acid, B-(4-acetylphenyl)-

CAS: 149104-90-5

Formula: C₈H₉BO₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 163.9663

Ref: IN-DA001LE0

4-Acetylphenylboronic acid

CAS: 149104-90-5

Formula: C₈H₉BO₃

Molecular weight: 163.97

Ref: 7W-GK4908

4-Acetylphenylboronic Acid (contains varying amounts of Anhydride)

CAS: 149104-90-5

Formula: C₈H₉BO₃

Color and Shape: White to Yellow to Orange powder to crystal

Molecular weight: 163.97

Ref: 3B-A1907

4-Acetylbenzeneboronic acid

CAS: 149104-90-5

4-Acetylbenzeneboronic acid

Formula: C₈H₉BO₃

Purity: 98%

Color and Shape: Pale yellow Solid

Molecular weight: 163.96626

Ref: 54-OR10313

4-Acetylphenylboronic acid

CAS: 149104-90-5

Formula: C₈H₉BO₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 163.97

Ref: 10-F021606

4-Acetylphenylboronic acid

CAS: 149104-90-5

4-Acetylphenylboronic acid

Formula: C₈H₉BO₃

Purity: 98%

Molecular weight: 163.97

Ref: IN-DG6444

4-Acetylphenylboronic Acid

Controlled Product

CAS: 149104-90-5

Applications 4-Acetylphenylboronic acid4-Acetylphenylboronic Acid is used in several metal catalyzed cross-coupling reaction studies.
References Saito, S., et al.: J. Org. Chem., 2, 8024 (1997); Sakai, M., et al.: Organomet., 16, 4229 (1997); Molander, G., et al.: J. Org. Chem., 68, 4302 (2003);

Formula: C₈H₉BO₃

Color and Shape: Neat

Molecular weight: 163.97

Ref: TR-A188840

4-Acetylphenylboronic acid

CAS: 149104-90-5

4-Acetylphenylboronic acid acts as an effective inhibitor targeting carbonic anhydrase II (CAII), displaying inhibitory concentrations (IC50) of 246 μM for bovine CAII (bCA II) and 281.40 μM for human CAII (hCA II).

Formula: C₈H₉BO₃

Color and Shape: Solid

Molecular weight: 163.97

Ref: TM-T88721