6-HYDROXY-2-NAPHTHALENEBORONICACID CAS:173194-95-1
Catalog Number | XD94768 |
Product Name | 6-HYDROXY-2-NAPHTHALENEBORONICACID |
CAS | 173194-95-1 |
Molecular Formula | C10H9BO3 |
Molecular Weight | 187.99 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
6-Hydroxy-2-naphthaleneboronic acid is an organic compound that belongs to the boronic acid family, with a hydroxyl group attached to a naphthalene ring. This compound exhibits several important effects and applications in various fields.One of the primary effects of 6-Hydroxy-2-naphthaleneboronic acid is its ability to act as a versatile building block in organic synthesis. Boronic acids are widely used in the formation of carbon-carbon bonds through a process called Suzuki-Miyaura cross-coupling reaction. This reaction allows for the synthesis of a wide range of complex organic molecules, including pharmaceuticals, agrochemicals, and materials with desired properties. The presence of the hydroxyl group on the naphthalene ring of this compound enables its participation in such reactions, expanding the scope of synthetic possibilities.Furthermore, 6-Hydroxy-2-naphthaleneboronic acid has been studied for its potential applications in the field of medicine. Boronic acids have a unique property of selectively binding to diols and biological molecules containing diol functional groups. This property has been exploited for the development of boronic acid-based drug delivery systems and sensors. Specifically, 6-Hydroxy-2-naphthaleneboronic acid can serve as a recognition element for glucose sensing, allowing for the detection and monitoring of glucose levels in biological fluids. This has implications in the management of diabetes and related disorders.Moreover, this compound has been found to exhibit antioxidant activity. Antioxidants play a crucial role in protecting cells from damage caused by free radicals and oxidative stress. The presence of the hydroxyl group in 6-Hydroxy-2-naphthaleneboronic acid enables it to scavenge free radicals and neutralize their harmful effects. This antioxidant activity makes it a potentially valuable ingredient in skincare products and dietary supplements aimed at promoting health and preventing oxidative damage.In summary, 6-Hydroxy-2-naphthaleneboronic acid exhibits important effects and applications in organic synthesis, medicine, and antioxidant research. Its versatility as a building block allows for the synthesis of complex organic molecules, while its ability to selectively bind to diols enables applications in drug delivery systems and glucose sensing. Additionally, its antioxidant activity makes it a potential ingredient in skincare and dietary products. Further research and exploration of its effects and applications are likely to uncover additional potentials in the fields of chemistry, medicine, and healthcare.