[4-(Cyclopropylmethoxy)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 cyclopropylmethoxy 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 cyclopropylmethoxy substituent can influence the compound's solubility, reactivity, and interaction with biological targets. Generally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds in organic synthesis. Additionally, the presence of the cyclopropyl group may impart unique steric and electronic properties, potentially enhancing the compound's efficacy in specific applications. Overall, [4-(cyclopropylmethoxy)phenyl]boronic acid is a versatile compound with significant implications in both synthetic and pharmaceutical chemistry.

[4-(cyclopropylmethoxy)phenyl]boronic acid

411229-67-9: boronic acid, B-[4-(cyclopropylmethoxy)phenyl]-

(4-(Cyclopropylmethoxy)phenyl)boronic acid

4-(Cyclopropylmethoxy)phenylboronic acid

4-(Cyclopropylmethoxy)benzeneboronic acid

CAS 411229-67-9: [4-(cyclopropylmethoxy)phenyl]boronic acid

(4-(Cyclopropylmethoxy)phenyl)boronic acid

Ref: IN-DA0073BQ

4-(Cyclopropylmethoxy)phenylboronic acid

Ref: 3D-LRA22967

4-(Cyclopropylmethoxy)benzeneboronic acid

Ref: 54-OR7194

(4-(Cyclopropylmethoxy)phenyl)boronic acid

Ref: 10-F377725