
CAS 1122568-09-5
:2-(2-Methoxyethoxy)phenylboronic acid
Description:
2-(2-Methoxyethoxy)phenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a methoxyethoxy group. This compound typically exhibits properties such as being a white to off-white solid at room temperature, with moderate solubility in polar organic solvents due to the presence of the methoxyethoxy moiety, which enhances its hydrophilicity. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and as a reagent in Suzuki coupling reactions. Additionally, the compound may exhibit interesting biological properties, as boronic acids can interact with biological molecules, potentially leading to applications in medicinal chemistry. Its stability and reactivity can be influenced by factors such as pH and the presence of other functional groups. Overall, 2-(2-Methoxyethoxy)phenylboronic acid is a versatile compound with significant utility in both synthetic and biological chemistry.
Formula:C9H13BO4
Synonyms:- Boronic acid, B-[2-(2-methoxyethoxy)phenyl]-
- [2-(2-METHOXYETHOXY)PHENYL]BORANEDIOL
- 2-(2-Methoxyethoxy)phenylboronic acid
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Found 4 products.
(2-(2-Methoxyethoxy)phenyl)boronic acid
CAS:Formula:C9H13BO4Purity:95%Color and Shape:SolidMolecular weight:196.00812-(2-Methoxyethoxy)phenylboronic acid
CAS:<p>2-(2-Methoxyethoxy)phenylboronic acid</p>Purity:98%Molecular weight:196.01g/mol2-(2-Methoxyethoxy)phenylboronic Acid
CAS:Controlled Product<p>Applications 2-(2-Methoxyethoxy)phenylboronic acid is a useful intermediate for organic synthesis.<br>References Adamczyk-Wozniak, A., et al.: J. Mol. Struct., 920, 430 (2009)<br></p>Formula:C9H13BO4Color and Shape:NeatMolecular weight:196.01



