CAS 1214723-26-8

3-(1-phenyl-1H-benzo[d]iMidazol-2-yl)phenylboronic acid

Description:

3-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenylboronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a phenylboronic acid moiety attached to a benzo[d]imidazole structure, which contributes to its potential biological activity and applications in medicinal chemistry. The presence of the imidazole ring suggests possible interactions with biological targets, making it of interest in drug development. Additionally, the compound's boronic acid functionality allows for participation in Suzuki coupling reactions, a valuable method in organic synthesis for forming carbon-carbon bonds. Its solubility and stability can vary depending on the pH and the presence of other functional groups. Overall, this compound's unique structural features and reactivity profile make it a subject of interest in both synthetic and medicinal chemistry.

Formula: C₁₉H₁₅BN₂O₂

Synonyms:

• B-[3-(1-phenyl-1H-benzimidazole-2-yl)phenyl]boronic acid
• 1-Phenyl-2-(phenyl-3-boromic acid)-benzinidazole

3-(1-phenyl-1H-benzo[d]iMidazol-2-yl)phenylboronic acid

CAS: 1214723-26-8

Formula: C₁₉H₁₅BN₂O₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 314.1456

Ref: IN-DA00150O

(3-(1-Phenyl-1H-benzo[d]imidazol-2-yl)phenyl)boronic acid

CAS: 1214723-26-8

(3-(1-Phenyl-1H-benzo[d]imidazol-2-yl)phenyl)boronic acid

Purity: 95%

Molecular weight: 314.15g/mol

Ref: 54-OR1054173

(3-(1-Phenyl-1H-benzo[d]imidazol-2-yl)phenyl)boronic acid

CAS: 1214723-26-8

Formula: C₁₉H₁₅BN₂O₂

Purity: 95.0%

Molecular weight: 314.15

Ref: 10-F328652