CAS 30418-59-8

3-Aminophenylboronic acid

Description:

3-Aminophenylboronic acid is an organic compound characterized by the presence of both an amino group and a boronic acid functional group attached to a phenyl ring. Its molecular structure features a boron atom bonded to a hydroxyl group and an aromatic ring that includes an amino substituent in the meta position. This compound is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the boronic acid group. 3-Aminophenylboronic acid is notable for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis, medicinal chemistry, and as a building block in the development of boron-containing materials. Additionally, it has potential applications in drug delivery systems and as a reagent in the synthesis of biologically active compounds. Its reactivity and functional versatility make it a valuable compound in both academic research and industrial applications.

Formula: C₆H₈BNO₂

InChI: InChI=1S/C6H8BNO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4,9-10H,8H2

InChI key: InChIKey=JMZFEHDNIAQMNB-UHFFFAOYSA-N

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

Synonyms:

• 3-Aminobenzeneboronic acid
• 3-Aminobenzeneboronicacid
• 3-Aminophenyl(dihydroxy)borane
• B-(3-Aminophenyl)boronic acid
• Benzeneboronic acid, m-amino-
• Boronic acid, (3-aminophenyl)-
• Boronic acid, B-(3-aminophenyl)-
• m-Aminobenzeneboronic acid
• m-Aminophenylboronic acid

3-Aminophenylboronic Acid Monohydrate (contains varying amounts of Anhydride)

CAS: 206658-89-1, 30418-59-8

Formula: C₆H₈BNO₂·H₂O

Purity: 97.0 to 116.0 %

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 154.97

Ref: 3B-A1281

3-Aminophenylboronic acid

CAS: 30418-59-8

Formula: C₆H₈BNO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 136.95

Ref: 10-F021277

3-Aminobenzeneboronic acid, 98%

CAS: 30418-59-8

3-Aminobenzeneboronic acid is used as an organic chemical synthesis intermediate. It is a boronic acid with potential use for biochemical research. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may ref

Formula: C₆H₈BNO₂

Purity: 98%

Molecular weight: 136.95

Ref: 02-H52909

3-Aminobenzeneboronic acid

CAS: 30418-59-8

Formula: C₆H₈BNO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 136.9442

Ref: IN-DA00302L

3-Aminophenylboronic acid

CAS: 30418-59-8

Formula: C₆H₈BNO₂

Purity: ≥ 97.0%

Color and Shape: White to yellow or brown powder or crystals

Molecular weight: 136.95

Ref: 7W-GK3705

3-Aminobenzeneboronic acid

CAS: 30418-59-8

3-Aminobenzeneboronic acid

Formula: C₆H₈BNO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 136.94421

Ref: 54-OR3933

3-Aminophenylboronic acid

CAS: 30418-59-8

(3-Aminophenyl)boronic acid

Formula: C₆H₈BNO₂

Purity: 98%

Molecular weight: 136.94

Ref: IN-DG3665

3-Aminophenylboronic acid

CAS: 30418-59-8

3-Aminophenylboronic acid is a chemical compound with the molecular formula of C6H5NH2B3O4. It has a phase transition temperature of 135.7 °C and is soluble in water. 3-Aminophenylboronic acid can be used to measure the concentration of dopamine in human serum, as well as other biological fluids, by using fluorescence probe methods or electrochemical impedance spectroscopy (EIS). 3-Aminophenylboronic acid reacts with ferrocene carboxylic acid to create an electrochemical current that can be measured using EIS.

Formula: C₆H₈BNO₂

Purity: Min. 98 Area-%

Color and Shape: Powder

Molecular weight: 136.94 g/mol

Ref: 3D-FA54894

3-Aminobenzeneboronic acid

CAS: 30418-59-8

3-Aminobenzeneboronic acid (3AB) is a colorless solid that is soluble in water and alcohol. It has a phase transition temperature of 170°C, a molar mass of 114.1 g/mol, and has two enantiomers. 3AB is a potent inhibitor of human basic fibroblast growth factor receptor 2 (HER2), which is a protein present on the cell surface that promotes tumor cell growth and survival in certain cancers, such as breast cancer. 3AB also inhibits prostate cancer cells by preventing sodium citrate from binding to the HER2 receptor. 3AB binds to human immunoglobulin G (IgG) with an affinity constant of 1 × 10 M and fluoresces under UV light at 355 nm. Kinetic data for the enzyme substrate dopamine shows that 3AB's inhibition can be attributed to competitive inhibition, where the enzyme competes with dopamine for access to its substrate. This compound has been shown to be useful in

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 136.94 g/mol

Ref: 3D-FA03380