B-[4-(Butylsulfinyl)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 butylsulfinyl group. This compound typically exhibits properties associated with 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 butylsulfinyl substituent enhances its solubility and may influence its reactivity and selectivity in chemical reactions. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. The presence of the sulfinyl group may also impart unique electronic properties, potentially affecting the compound's reactivity and interaction with biological targets. Overall, B-[4-(Butylsulfinyl)phenyl]boronic acid is a versatile compound with applications in synthetic organic chemistry and potential implications in drug development.

B-[4-(Butylsulfinyl)phenyl]boronic acid

1217501-01-3: Boronic acid, B-[4-(butylsulfinyl)phenyl]-, B-[4-(Butylsulfinyl)phenyl]boronic acid

CAS 1217501-01-3: B-[4-(Butylsulfinyl)phenyl]boronic acid

(4-(Butylsulfinyl)phenyl)boronic acid

Ref: 10-F228510

Boronic acid, B-[4-(butylsulfinyl)phenyl]-

Ref: IN-DA0015RN

4-(Butylsulfinyl)phenylboronic acid

Ref: 54-OR360503

4-(Butylsulfinyl)phenylboronic acid

Ref: 3D-SYB50101