1H-1,2,3-TRIAZOLE-4-BORONIC ACID
95%
- Product Code: 89521
CAS:
2225172-22-3
| Molecular Weight: | 112.88306 g./mol | Molecular Formula: | C₂H₄BN₃O₂ |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
1H-1,2,3-Triazole-4-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a versatile building block due to its boronic acid group, which facilitates coupling with aryl or vinyl halides in the presence of a palladium catalyst. Its triazole ring also contributes to its utility in medicinal chemistry, where it is incorporated into drug candidates to enhance biological activity and stability. Additionally, it is employed in the development of fluorescent probes and sensors, leveraging its ability to interact with specific biological or chemical targets. Its applications extend to polymer chemistry, where it is used to modify polymers for improved properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿18,900.00 |
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| 0.025 | 10-20 days | ฿54,000.00 |
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1H-1,2,3-TRIAZOLE-4-BORONIC ACID
1H-1,2,3-Triazole-4-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a versatile building block due to its boronic acid group, which facilitates coupling with aryl or vinyl halides in the presence of a palladium catalyst. Its triazole ring also contributes to its utility in medicinal chemistry, where it is incorporated into drug candidates to enhance biological activity and stability. Additionally, it is employed in the development of fluorescent probes and sensors, leveraging its ability to interact with specific biological or chemical targets. Its applications extend to polymer chemistry, where it is used to modify polymers for improved properties.
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