B-[3-(2-Fluoroethoxy)phenyl]boronic 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 2-fluoroethoxy group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the fluorinated ethoxy group can enhance the compound's lipophilicity and influence its reactivity and biological activity. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. The compound's solubility, stability, and reactivity can be influenced by the specific substituents on the phenyl ring and the boronic acid group. Overall, B-[3-(2-Fluoroethoxy)phenyl]boronic acid represents a versatile building block in the development of pharmaceuticals and agrochemicals.

B-[3-(2-Fluoroethoxy)phenyl]boronic acid

2096332-11-3: B-[3-(2-Fluoroethoxy)phenyl]boronic acid, Boronic acid, B-[3-(2-fluoroethoxy)phenyl]-

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CAS 2096332-11-3: B-[3-(2-Fluoroethoxy)phenyl]boronic acid

3-(2-Fluoroethoxy)phenylboronic acid

Ref: 3D-WID33211

3-(2-Fluoroethoxy)phenylboronic acid

Ref: IN-DA01EHEC

(3-(2-Fluoroethoxy)phenyl)boronic acid

Ref: 10-F612754

3-(2-Fluoroethoxy)phenylboronic acid

Ref: 54-PC901356