(2S,5R)-Ethyl 5-[(benzyloxy)amino]piperidine-2-carboxylate oxalate CAS: 1416134-48-9
Catalog Number | XD93941 |
Product Name | (2S,5R)-Ethyl 5-[(benzyloxy)amino]piperidine-2-carboxylate oxalate |
CAS | 1416134-48-9 |
Molecular Formula | C17H24N2O7 |
Molecular Weight | 368.39 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
(2S,5R)-Ethyl 5-[(benzyloxy)amino]piperidine-2-carboxylate oxalate is a chemical compound used in organic synthesis and pharmaceutical research. Its unique structure makes it valuable in the development and synthesis of various biologically active compounds.One of the main applications of (2S,5R)-Ethyl 5-[(benzyloxy)amino]piperidine-2-carboxylate oxalate is in medicinal chemistry. It serves as a precursor in the synthesis of piperidine-based compounds that may have potential therapeutic uses. The piperidine moiety is a common structural element found in numerous pharmaceutical drugs due to its ability to interact with a variety of biological targets.Researchers often modify the benzyl group attached to the piperidine ring to introduce desired pharmacological properties to the final compounds. This can involve the use of different protecting groups or substituting the benzyl group with other functional groups. The versatility of (2S,5R)-Ethyl 5-[(benzyloxy)amino]piperidine-2-carboxylate oxalate allows chemists to incorporate diverse functionalities, enhancing the potential for activity against specific diseases or targets.Additionally, the oxalate counterion of the compound aids in its purification and handling. The oxalate salt form provides improved solubility in various organic solvents, making it easier for researchers to work with the compound during synthesis and purification processes.The compound's synthetic applications extend beyond medicinal chemistry. It can be used as an intermediate in the preparation of other complex molecules, such as natural product derivatives or materials with specific functional groups. The piperidine scaffold is prevalent in many biologically active natural products, making it an attractive target for drug discovery and development. By utilizing (2S,5R)-Ethyl 5-[(benzyloxy)amino]piperidine-2-carboxylate oxalate as a starting material, scientists can access a wide range of piperidine-based compounds for further investigation.In conclusion, (2S,5R)-Ethyl 5-[(benzyloxy)amino]piperidine-2-carboxylate oxalate is a versatile compound utilized in organic synthesis and pharmaceutical research. Its piperidine-based structure allows for the synthesis of diverse compounds, with potential applications in medicinal chemistry and drug discovery. The compound's oxalate salt form enhances its solubility and ease of handling during synthesis and purification processes. Overall, (2S,5R)-Ethyl 5-[(benzyloxy)amino]piperidine-2-carboxylate oxalate plays a crucial role in the development of biologically active molecules and serves as an important tool for chemists and researchers in the field of synthetic organic chemistry.