6-(Benzyloxy)-2-naphthylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a naphthalene ring system. This compound features a benzyloxy substituent at the 6-position of the naphthalene, which enhances its solubility and reactivity. 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 medicinal chemistry. The compound typically exhibits moderate stability under ambient conditions but may be sensitive to moisture due to the presence of the boronic acid moiety. It is often utilized in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, its structural features may contribute to its potential biological activity, making it a candidate for further research in drug development. Overall, 6-(Benzyloxy)-2-naphthylboronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.

6-(Benzyloxy)-2-naphthylboronic acid

152915-83-8: [6-(Benzyloxy)Naphthalen-2-Yl]Boronic Acid

CAS 152915-83-8: 6-(Benzyloxy)-2-naphthylboronic acid

6-(Benzyloxy)-2-naphthylboronic acid

Ref: 54-OR360218

6-Benzyloxy-2-naphthylboronic acid

Ref: 10-F225408

6-(BENZYLOXY)-2-NAPHTHYLBORONIC ACID

Ref: IN-DA00APW1