(1H-Benzo[d][1,2,3]triazol-5-yl)boronic acid
95%
- Product Code: 195552
CAS:
183282-45-3
| Molecular Weight: | 162.94 g./mol | Molecular Formula: | C₆H₆BN₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD10697877 | |
| Melting Point: | Boiling Point: | 557.9±42.0°C at 760 mmHg | |
| Density: | Storage Condition: | -20°C, stored in inert gas |
Product Description:
Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions where it enables the formation of carbon-carbon bonds. Its boronic acid group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in constructing complex organic molecules. Additionally, the triazole ring enhances stability and can participate in hydrogen bonding, which is beneficial in medicinal chemistry for improving binding affinity and pharmacokinetic properties. It is also employed in materials science for developing fluorescent probes and sensors due to the inherent photophysical properties of the triazole-boronate system.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿37,660.00 |
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(1H-Benzo[d][1,2,3]triazol-5-yl)boronic acid
Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions where it enables the formation of carbon-carbon bonds. Its boronic acid group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in constructing complex organic molecules. Additionally, the triazole ring enhances stability and can participate in hydrogen bonding, which is beneficial in medicinal chemistry for improving binding affinity and pharmacokinetic properties. It is also employed in materials science for developing fluorescent probes and sensors due to the inherent photophysical properties of the triazole-boronate system.
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