4-(2-Phenyl-1H-benzimidazol-1-yl)phenylboronic Acid
98%, containing different amounts of acid anhydride
- Product Code: 90368
CAS:
867044-33-5
| Molecular Weight: | 314.15 g./mol | Molecular Formula: | C₁₉H₁₅BN₂O₂ |
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| EC Number: | MDL Number: | MFCD11977298 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of complex organic molecules. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to interact with specific analytes. Its benzimidazole moiety also contributes to its use in designing compounds with potential biological activity, such as antimicrobial or anticancer agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | $343.49 |
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4-(2-Phenyl-1H-benzimidazol-1-yl)phenylboronic Acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of complex organic molecules. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to interact with specific analytes. Its benzimidazole moiety also contributes to its use in designing compounds with potential biological activity, such as antimicrobial or anticancer agents.
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