For research use only. Not for therapeutic Use.
5,6,7,8-Tetrahydronaphthalen-2-ylboronic acid(CAT: L031088) is an organoboron compound featuring a boronic acid functional group attached to a tetrahydronaphthalene ring system. This structure is commonly used in Suzuki-Miyaura cross-coupling reactions, a popular method in organic synthesis for constructing carbon-carbon bonds. The tetrahydronaphthalene ring provides a partially saturated, stable aromatic framework, which can contribute to enhanced lipophilicity and bioavailability in synthesized compounds. This compound serves as a valuable intermediate in the development of pharmaceuticals, agrochemicals, and advanced materials, particularly for applications requiring functionalized aromatic systems. Its boronic acid group facilitates its role in constructing complex molecules, often for drug design and medicinal chemistry applications.
Catalog Number | L031088 |
CAS Number | 405888-56-4 |
Molecular Formula | C10H13BO2 |
Purity | ≥95% |
IUPAC Name | 5,6,7,8-tetrahydronaphthalen-2-ylboronic acid |
InChI | InChI=1S/C10H13BO2/c12-11(13)10-6-5-8-3-1-2-4-9(8)7-10/h5-7,12-13H,1-4H2 |
InChIKey | LMASCDCJPOZWMK-UHFFFAOYSA-N |