D-Phenyl Glycline Dane Salt CAS:961-69-3

D-Phenylglycine Dane salt is a chiral amino acid derivative that combines the characteristics of D-phenylglycine with enhanced solubility and stability provided by its salt form. With the molecular formula C8H10N1O2·HCl, this compound features a phenyl group attached to the second carbon of the glycine backbone, leading to distinct physicochemical properties that facilitate its use in various applications, predominantly within the fields of pharmaceuticals and organic synthesis. One of the primary applications of D-phenylglycine Dane salt lies in its role as a building block for synthesizing bioactive compounds. Its unique structure allows chemists to incorporate it into larger molecular frameworks, leading to the development of new drugs targeting various diseases. Research has highlighted its potential in creating analgesics and anti-inflammatory agents, suggesting that derivatives of D-phenylglycine may provide effective treatments for pain management and inflammatory conditions. Its ability to interact with specific biological pathways makes it a candidate for further exploration in drug discovery. Additionally, D-phenylglycine Dane salt serves as a crucial intermediate in asymmetric synthesis, where the production of specific enantiomers is vital for developing effective pharmaceuticals. Its application enables chemists to achieve higher selectivity and activity in their synthetic routes, reducing the likelihood of side effects associated with racemic mixtures. The compound's importance extends beyond medicinal chemistry; it is also employed in analytical methods, such as chromatography, where its chiral nature can be utilized to separate enantiomers of other compounds effectively. In summary, D-Phenylglycine Dane salt is a significant compound in organic and medicinal chemistry. Its dual role as both a precursor for drug synthesis and a potential therapeutic agent emphasizes its relevance in advancing medical science. Continued research into its applications and biological activities will likely unveil additional therapeutic opportunities and enhance our understanding of this important amino acid derivative.