(3-(2-(Dimethylamino)ethoxy)phenyl)boronic acid
98%
- Product Code: 65459
CAS:
1139717-84-2
| Molecular Weight: | 209.05 g./mol | Molecular Formula: | C₁₀H₁₆BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11103731 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in the development of pharmaceuticals. It is often employed in Suzuki-Miyaura cross-coupling reactions, which are crucial for creating carbon-carbon bonds in drug discovery and material science. This compound is also utilized in the synthesis of boron-containing compounds that have potential applications in cancer therapy, as boron neutron capture therapy (BNCT) agents. Additionally, it serves as a building block in the development of sensors and probes for detecting biological molecules due to its boronic acid functionality, which can selectively bind to diols and sugars.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿35,150.00 |
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(3-(2-(Dimethylamino)ethoxy)phenyl)boronic acid
Used in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in the development of pharmaceuticals. It is often employed in Suzuki-Miyaura cross-coupling reactions, which are crucial for creating carbon-carbon bonds in drug discovery and material science. This compound is also utilized in the synthesis of boron-containing compounds that have potential applications in cancer therapy, as boron neutron capture therapy (BNCT) agents. Additionally, it serves as a building block in the development of sensors and probes for detecting biological molecules due to its boronic acid functionality, which can selectively bind to diols and sugars.
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