| Chemical Name: | (6-(Benzyloxy)-2,3-difluorophenyl)boronic acid |
| CAS Number: | 1451393-19-3 |
| Product Number: | AG00AM5Y(AGN-PC-0WAMO3) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C13H11BF2O3 |
| Molecular Weight: | 264.0324 |
The (6-(Benzyloxy)-2,3-difluorophenyl)boronic acid is a versatile compound commonly employed in chemical synthesis as a key building block. Its unique structure and reactivity make it an essential tool for organic chemists in various processes.In chemical synthesis, this compound serves as a valuable component for Suzuki-Miyaura cross-coupling reactions. By utilizing this boronic acid derivative as a coupling partner, chemists can efficiently and selectively construct C-C bonds, enabling the synthesis of complex organic molecules. Its boronic acid functionality plays a crucial role in facilitating these cross-coupling reactions by forming stable boronates with aryl halides or triflates under palladium-catalyzed conditions.Furthermore, the benzyl ether moiety in this compound serves as a protecting group, allowing chemists to selectively control the reactivity of the phenyl boronic acid group. This feature enables the sequential deprotection and functionalization of the boronic acid group, providing a strategic advantage in multi-step organic synthesis.Overall, the (6-(Benzyloxy)-2,3-difluorophenyl)boronic acid plays a vital role in modern chemical synthesis strategies, offering chemists a powerful tool for the construction of complex organic molecules with high efficiency and selectivity.
![O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]](https://img.angenechemical.com/storage/3a59/3a5932eec850ab245f6f4d4a7f9497f9.png)
(Cl)Cl)c1c(C)cc(cc1C)C](https://img.angenechemical.com/storage/6693/66939a3f08a27d2b6717c3194e00970b.png)
