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(2S,5R)-Ethyl 5-[(benzyloxy)amino]piperidine-2-carboxylate oxalate CAS:1416134-48-9

(2S,5R)-Ethyl 5-[(benzyloxy)amino]piperidine-2-carboxylate oxalate is a chemical compound utilized in organic synthesis and pharmaceutical research. With the molecular formula C17H24N2O5·C2H2O4, it exhibits specific structural features that make it valuable in various chemical and biological applications.


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Application and Effect:

(2S,5R)-Ethyl 5-[(benzyloxy)amino]piperidine-2-carboxylate oxalate plays a significant role in organic synthesis and pharmaceutical research due to its unique chemical properties. In organic synthesis, it serves as a versatile building block for the construction of complex molecules and pharmaceutical intermediates. Its piperidine ring and carboxylate functional group enable it to participate in various chemical transformations, including acylation, alkylation, and cyclization reactions, facilitating the synthesis of diverse organic compounds. Furthermore, (2S,5R)-Ethyl 5-[(benzyloxy)amino]piperidine-2-carboxylate oxalate finds utility in pharmaceutical research as a potential drug candidate or pharmacological probe. Its structural resemblance to certain bioactive molecules makes it a valuable scaffold for the design and synthesis of novel therapeutics targeting various biological pathways and disease conditions. Moreover, this compound exhibits pharmacological properties that may be explored for therapeutic applications. Research studies aim to elucidate its pharmacokinetic profiles, pharmacodynamic effects, and potential therapeutic indications, paving the way for the development of new drugs for the treatment of neurological disorders, psychiatric conditions, or other medical ailments. Additionally, (2S,5R)-Ethyl 5-[(benzyloxy)amino]piperidine-2-carboxylate oxalate serves as a valuable research tool in chemical biology and medicinal chemistry. Its ability to modulate specific biological targets or pathways allows researchers to investigate molecular mechanisms underlying physiological processes or disease states, facilitating drug discovery and development efforts. Furthermore, this compound may find applications in asymmetric synthesis and chiral resolution processes, owing to its stereospecific configuration. Its chiral nature makes it useful in the synthesis of enantiomerically pure compounds, which are essential in pharmaceuticals, agrochemicals, and fine chemical industries. Overall, the multifaceted nature of (2S,5R)-Ethyl 5-[(benzyloxy)amino]piperidine-2-carboxylate oxalate makes it invaluable in organic synthesis, pharmaceutical research, chemical biology, and medicinal chemistry. Its role as a building block, drug candidate, pharmacological tool, and chiral auxiliary underscores its significance in advancing scientific knowledge and innovation in the field of chemistry and drug discovery.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C17H24N2O5·C2H2O4
Assay 99%
Appearance white powder
CAS No.  1416134-48-9
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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