4-(1-phenyl-1H-benzo[d]iMidazol-2-yl)phenylboronic acid(PBIB)
1-phenyl-2-(phenyl-4-boronic acid)-benzimidazole
CAS: 952514-79-3
Molecular Formula: C19H15BN2O2
4-(1-phenyl-1H-benzo[d]iMidazol-2-yl)phenylboronic acid(PBIB) - Names and Identifiers
4-(1-phenyl-1H-benzo[d]iMidazol-2-yl)phenylboronic acid(PBIB) - Physico-chemical Properties
| Molecular Formula | C19H15BN2O2 |
| Molar Mass | 314.15 |
| Density | 1.21±0.1 g/cm3(Predicted) |
| Boling Point | 572.6±60.0 °C(Predicted) |
| pKa | 8.47±0.17(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
4-(1-phenyl-1H-benzo[d]iMidazol-2-yl)phenylboronic acid(PBIB) - Introduction
1-phenyl-2-(phenyl-4-boronic acid)-benzimidazole is a compound containing a benzene ring and a benzimidazole structure. Its molecular formula is C18H14BN3O2.
The compound is a solid with a white to off-white crystal morphology. Its melting point is 173-176 degrees Celsius. It is relatively stable at room temperature, but not stable under strong acid and alkali conditions. It is soluble in organic solvents.
1-phenyl-2-(phenyl-4-boronic acid)-benzimidazole is an important intermediate in the field of organic synthesis. It is often used as a catalyst support for aldehyde condensation reactions in organic synthesis. It can be reacted with various organic compounds, for example, for the alkylation reaction of aryl compounds, coupling reaction and oxygen kinetic reaction, etc. In addition, it also has potential applications in pharmaceutical research and coordination chemistry.
The method of preparing 1-phenyl-2-(phenyl-4-boronic acid)-benzimidazole is usually achieved by reacting phenylboronic acid with a benzimidazole compound. The reaction may be carried out in a suitable organic solvent and catalyzed by a suitable catalyst. The reaction conditions including temperature, reaction time, reactant ratio and so on need to be optimized.
With regard to safety information, the toxicity and danger of 1-phenyl-2-(phenyl-4-boronic acid)-benzimidazole has not been fully studied and evaluated. However, as an organic compound, it should be considered as a potentially hazardous substance. During handling and use, appropriate protective measures should be taken, such as wearing chemical protective gloves, eye protection, etc. Seal the container and keep it properly to avoid contact with oxidants and strong acids. If ingestion or skin contact, should promptly seek medical attention.
The compound is a solid with a white to off-white crystal morphology. Its melting point is 173-176 degrees Celsius. It is relatively stable at room temperature, but not stable under strong acid and alkali conditions. It is soluble in organic solvents.
1-phenyl-2-(phenyl-4-boronic acid)-benzimidazole is an important intermediate in the field of organic synthesis. It is often used as a catalyst support for aldehyde condensation reactions in organic synthesis. It can be reacted with various organic compounds, for example, for the alkylation reaction of aryl compounds, coupling reaction and oxygen kinetic reaction, etc. In addition, it also has potential applications in pharmaceutical research and coordination chemistry.
The method of preparing 1-phenyl-2-(phenyl-4-boronic acid)-benzimidazole is usually achieved by reacting phenylboronic acid with a benzimidazole compound. The reaction may be carried out in a suitable organic solvent and catalyzed by a suitable catalyst. The reaction conditions including temperature, reaction time, reactant ratio and so on need to be optimized.
With regard to safety information, the toxicity and danger of 1-phenyl-2-(phenyl-4-boronic acid)-benzimidazole has not been fully studied and evaluated. However, as an organic compound, it should be considered as a potentially hazardous substance. During handling and use, appropriate protective measures should be taken, such as wearing chemical protective gloves, eye protection, etc. Seal the container and keep it properly to avoid contact with oxidants and strong acids. If ingestion or skin contact, should promptly seek medical attention.
Last Update：2024-04-09 20:45:29
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CAS: 952514-79-3
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CAS: 952514-79-3
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Mobile: 18021002903
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