(4-(1-Phenyl-1H-benzo[d]imidazol-2-yl)phenyl)boronic acid
99%
- Product Code: 224340
CAS:
952514-79-3
| Molecular Weight: | 314.1500 g./mol | Molecular Formula: | C₁₉H₁₅BN₂O₂ |
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| EC Number: | MDL Number: | MFCD11045057 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, inert gas |
Product Description:
Used in organic synthesis as a key building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds important in pharmaceuticals and agrochemicals. Its boronic acid functionality allows for efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of fluorescent materials and sensors due to the presence of the benzimidazole moiety, which can act as a signaling unit. Also utilized in medicinal chemistry for constructing libraries of bioactive molecules, particularly those targeting kinase inhibitors and anticancer agents. Its structural rigidity and ability to participate in hydrogen bonding make it suitable for designing compounds with enhanced binding affinity and selectivity.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 1g | 10-20 days | ฿1,240.00 |
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| 5g | 10-20 days | ฿4,830.00 |
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(4-(1-Phenyl-1H-benzo[d]imidazol-2-yl)phenyl)boronic acid
Used in organic synthesis as a key building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds important in pharmaceuticals and agrochemicals. Its boronic acid functionality allows for efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of fluorescent materials and sensors due to the presence of the benzimidazole moiety, which can act as a signaling unit. Also utilized in medicinal chemistry for constructing libraries of bioactive molecules, particularly those targeting kinase inhibitors and anticancer agents. Its structural rigidity and ability to participate in hydrogen bonding make it suitable for designing compounds with enhanced binding affinity and selectivity.
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