Pinacol 3-(benzamido) phenylboronic acid
95%
- Product Code: 44615
CAS:
1330596-14-9
| Molecular Weight: | 323.20 g./mol | Molecular Formula: | C₁₉H₂₂BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22494317 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20℃, inert gas |
Product Description:
Used in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in cross-coupling reactions like Suzuki-Miyaura coupling, which is widely applied in the pharmaceutical industry for creating carbon-carbon bonds. Its boronic acid group enables selective binding to diols and sugars, making it valuable in carbohydrate chemistry and sensor development. Additionally, it serves as a building block in the synthesis of bioactive compounds, including potential drug candidates targeting diseases such as cancer and inflammation. Its phenylboronic acid moiety is also utilized in materials science for designing functional polymers and hydrogels.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €322.20 |
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| 0.250 | 10-20 days | €538.03 |
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| 1.000 | 10-20 days | €1,075.83 |
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Pinacol 3-(benzamido) phenylboronic acid
Used in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in cross-coupling reactions like Suzuki-Miyaura coupling, which is widely applied in the pharmaceutical industry for creating carbon-carbon bonds. Its boronic acid group enables selective binding to diols and sugars, making it valuable in carbohydrate chemistry and sensor development. Additionally, it serves as a building block in the synthesis of bioactive compounds, including potential drug candidates targeting diseases such as cancer and inflammation. Its phenylboronic acid moiety is also utilized in materials science for designing functional polymers and hydrogels.
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