4-(2-(Dimethylamino)ethoxy)-3-fluorophenylboronic acid
98%
- Product Code: 90335
CAS:
944279-23-6
| Molecular Weight: | 227.05 g./mol | Molecular Formula: | C₁₀H₁₅BFNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28400495 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent to form carbon-carbon bonds. Its structure, featuring a fluorine atom and a dimethylaminoethoxy group, enhances its reactivity and selectivity in these reactions, making it valuable for constructing complex organic molecules. It is also employed in the development of pharmaceuticals, where it serves as a key intermediate in synthesizing biologically active compounds. Additionally, its unique properties make it suitable for research in material science, particularly in designing advanced materials with specific electronic or structural characteristics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿109,960.00 |
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4-(2-(Dimethylamino)ethoxy)-3-fluorophenylboronic acid
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent to form carbon-carbon bonds. Its structure, featuring a fluorine atom and a dimethylaminoethoxy group, enhances its reactivity and selectivity in these reactions, making it valuable for constructing complex organic molecules. It is also employed in the development of pharmaceuticals, where it serves as a key intermediate in synthesizing biologically active compounds. Additionally, its unique properties make it suitable for research in material science, particularly in designing advanced materials with specific electronic or structural characteristics.
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