CAS 63503-60-6

3-Chlorophenylboronic acid

Description:

3-Chlorophenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a chlorinated phenyl ring. Its molecular structure features a boron atom bonded to a hydroxyl group and a phenyl group that has a chlorine substituent at the meta position. This compound is typically a white to off-white solid and is soluble in polar organic solvents. It is known for its utility in organic synthesis, particularly in Suzuki coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. The presence of the boronic acid group allows for the formation of stable complexes with diols, making it useful in various applications, including drug development and materials science. Additionally, 3-chlorophenylboronic acid can exhibit biological activity, which may be of interest in medicinal chemistry. Safety precautions should be taken when handling this compound, as boronic acids can be irritants and may pose environmental hazards.

Formula: C₆H₆BClO₂

InChI: InChI=1/C6H6BClO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4,9-10H

SMILES: c1cc(cc(c1)Cl)B(O)O

Synonyms:

• Rarechem Ah Pb 0179
• M-Chlorophenylboronic Acid
• Akos Brn-0010
• 3-Chlorophenylbornic Acid
• 3-Chlorobenzeneboronic Acid
• 3-Chlorobenzeneboronic Acid / 3-Chlorophenylboronic Acid
• 3-Chlorophenylboronic Acid 98%
• 3-Chloro benzene boronic acid:

3-Chlorophenylboronic Acid (contains varying amounts of Anhydride)

CAS: 63503-60-6

Formula: C₆H₆BClO₂

Purity: 97.0 to 114.0 %

Color and Shape: White to Almost white powder to crystal

Molecular weight: 156.37

Ref: 3B-C1613

3-Chlorobenzeneboronic acid, 97%

CAS: 63503-60-6

It is employed as a reactant involved in 1,4-conjugate addition reactions with ethenesulfonamides to form arylethanesulfonamides, Suzuki-Miyaura reactions with dibromotrifluoromethylbenzene, cross-coupling reactions with diazoesters3 or potassium cyanate. It is involved in the synthesis of biarylket

Formula: C₆H₆BClO₂

Purity: 97%

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

Molecular weight: 156.37

Ref: 02-B24444

3-Chlorobenzeneboronic Acid

CAS: 63503-60-6

Formula: C₆H₆BClO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 156.3746

Ref: IN-DA0033O8

3-Chlorophenylboronic acid

CAS: 63503-60-6

Formula: C₆H₆BClO₂

Molecular weight: 156.38

Ref: 7W-GK3131

3-Chlorophenylboronic acid

CAS: 63503-60-6

3-Chlorophenylboronic acid: key for prolyl hydroxylase inhibitors, diverse compounds synthesis; IC50 0.418 µM for LYPLA2.

Formula: C₆H₆BClO₂

Purity: 98.62%

Color and Shape: Solid

Molecular weight: 156.37

Ref: TM-T77514

3-Chlorobenzeneboronic acid

CAS: 63503-60-6

3-Chlorobenzeneboronic acid

Formula: C₆H₆BClO₂

Purity: 98%

Color and Shape: off white solid

Molecular weight: 156.37g/mol

Ref: 54-OR6642

3-Chlorophenylboronic acid

CAS: 63503-60-6

3-Chlorophenylboronic acid

Purity: ≥98%

Molecular weight: 156.37g/mol

Ref: 54-BUP19883

3-Chlorobenzeneboronic acid

CAS: 63503-60-6

Formula: C₆H₆BClO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 156.37

Ref: 10-F010985

3-Chlorophenylboronic Acid

Controlled Product

CAS: 63503-60-6

Applications 3-Chlorophenylboronic acid is a useful research chemical, a useful reagent for Suzuki-Miyaura cross-coupling reactions.
References Savitha, B., et al.: J. Heterocycl. Chem., 55, 2277 (2018); Liu, K., et al.: Eur. J. Org. Chem., 34, 4769 (2018)

Formula: C₆H₆BClO₂

Color and Shape: Neat

Molecular weight: 156.375

Ref: TR-C596510

Vismodegib Impurity 10

CAS: 63503-60-6

Formula: C₆H₆BClO₂

Molecular weight: 156.37

Ref: ST-EA-CP-V25009