3-(tert-Butoxycarbonyl)phenylboronic Acid
98%
- Product Code: 90034
CAS:
220210-56-0
| Molecular Weight: | 222.05 g./mol | Molecular Formula: | C₁₁H₁₅BO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 96-102°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group facilitates the coupling with aryl or vinyl halides, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the preparation of biaryl compounds, which are essential in drug discovery and development. The tert-butoxycarbonyl (Boc) protecting group enhances stability and selectivity during reactions, making it a valuable tool in multi-step synthetic processes. It is also utilized in the development of sensors and molecular recognition systems due to its ability to interact with diols and other functional groups.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97.5-100 |
| Appearance | WHITE TO OFF-WHITE CRYSTALS OR POWDER |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿288.00 |
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| 5.000 | 10-20 days | ฿918.00 |
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| 25.000 | 10-20 days | ฿3,195.00 |
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3-(tert-Butoxycarbonyl)phenylboronic Acid
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group facilitates the coupling with aryl or vinyl halides, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the preparation of biaryl compounds, which are essential in drug discovery and development. The tert-butoxycarbonyl (Boc) protecting group enhances stability and selectivity during reactions, making it a valuable tool in multi-step synthetic processes. It is also utilized in the development of sensors and molecular recognition systems due to its ability to interact with diols and other functional groups.
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