CAS 71597-85-8

(4-Hydroxyphenyl)boronic acid

Description:

(4-Hydroxyphenyl)boronic acid, with the CAS number 71597-85-8, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a para-hydroxyphenyl moiety. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the hydroxyl group. It exhibits properties typical of boronic acids, including the ability to form reversible complexes with diols and sugars, making it useful in various applications, particularly in organic synthesis and medicinal chemistry. The hydroxyl group enhances its reactivity and solubility, while the boronic acid functionality allows for participation in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. Additionally, (4-Hydroxyphenyl)boronic acid has potential applications in the development of sensors and drug delivery systems due to its ability to interact with biological molecules. Its stability and reactivity make it a valuable compound in both research and industrial settings.

Formula: C₆H₇BO₃

InChI: InChI=1S/C6H7BO3/c8-6-3-1-5(2-4-6)7(9)10/h1-4,8-10H

InChI key: InChIKey=COIQUVGFTILYGA-UHFFFAOYSA-N

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

Synonyms:

• (4-Hydroxyphenyl)Boronic Acid
• (p-Hydroxyphenyl)boronic acid
• 4-Boronophenol
• 4-Hydroxyphenylboronic acid
• B-(4-Hydroxyphenyl)boronic acid
• Benzeneboronic acid, p-hydroxy-
• Boronic acid, (4-hydroxyphenyl)-
• Boronic acid, B-(4-hydroxyphenyl)-

4-Hydroxyphenylboronic Acid (contains varying amounts of Anhydride)

CAS: 71597-85-8

Formula: C₆H₇BO₃

Purity: 97.0 to 115.0 %

Color and Shape: White to Gray to Brown powder to crystal

Molecular weight: 137.93

Ref: 3B-H1228

4-Hydroxybenzeneboronic acid, 97%

CAS: 71597-85-8

4-Hydroxybenzeneboronic acid is used for Suzuki-Miyaura coupling and Stille coupling and potential for introducing different alkyl groups, palladium-catalyzed aminocarbonylation and cross-coupling reactions, bio-supported palladium nanoparticles as phosphine-free catalyst for Suzuki reaction in wate

Formula: C₆H₇BO₃

Purity: 97%

Color and Shape: Crystals or powder or crystalline powder or granules, White to cream to brown to gray

Molecular weight: 137.93

Ref: 02-L15594

4-Hydroxyphenylboronic acid

CAS: 71597-85-8

Formula: C₆H₇BO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 137.9290

Ref: IN-DA00342G

4-Hydroxyphenylboronic acid

CAS: 71597-85-8

Formula: C₆H₇BO₃

Molecular weight: 137.93

Ref: 7W-GK8854

4-Hydroxyphenylboronic acid

CAS: 71597-85-8

Purity: 98%

Molecular weight: 137.929

Ref: FT-H5363

4-Hydroxybenzeneboronic acid

CAS: 71597-85-8

4-Hydroxybenzeneboronic acid

Formula: C₆H₇BO₃

Purity: 97%

Color and Shape: white to off white solid

Molecular weight: 137.93g/mol

Ref: 54-OR10505

4-Hydroxybenzeneboronic Acid

Controlled Product

CAS: 71597-85-8

Formula: C₆H₇BO₃

Color and Shape: Neat

Molecular weight: 137.93

Ref: TR-H949555

4-Hydroxyphenylboronic acid

CAS: 71597-85-8

Formula: C₆H₇BO₃

Purity: 98%

Color and Shape: Solid, Chunks or Crystalline Powder

Molecular weight: 137.93

Ref: 10-F050303

4-Hydroxyphenylboronic acid

CAS: 71597-85-8

4-Hydroxyphenylboronic acid is a potential anticancer agent that has been studied in vitro and in vivo. It has been shown to inhibit the activity of p-glycoprotein, which is a protein that pumps drugs out of cells, and it is also an inhibitor of lipid kinase. 4-Hydroxyphenylboronic acid binds to the ATP binding site of the enzyme and forms covalent bonds with Lys residues on the enzyme, inhibiting its function. The compound can be detected at low concentrations using fluorescence or chemiluminescence techniques. This compound may have therapeutic benefits for antimicrobial agents as well as for cancer treatment.

Formula: C₆H₇BO₃

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 137.93 g/mol

Ref: 3D-FH10224