521302-69-2 Usage
Description
(E)-tert-butyl 4-(1-amino-3-ethoxy-3-oxoprop-1-enyl)piperidine-1-carboxylate is a chemical compound with the molecular formula C17H30N2O4. It is a piperidine derivative featuring a tert-butyl ester group and an ethoxyoxopropenylamino side chain. (E)-tert-butyl 4-(1-amino-3-ethoxy-3-oxoprop-1-enyl)piperidine-1-carboxylate holds potential in pharmaceutical research and development, as well as in the synthesis of organic compounds. Its unique structure and functional groups suggest possible biological activity, making it a candidate for the development of new drugs or as a building block for synthesizing complex organic molecules. Further research and testing are required to explore its full potential uses and properties.
Uses
Used in Pharmaceutical Research and Development:
(E)-tert-butyl 4-(1-amino-3-ethoxy-3-oxoprop-1-enyl)piperidine-1-carboxylate is used as a chemical intermediate for the development of new drugs. Its specific structure and functional groups may contribute to its biological activity, which can be harnessed to create novel therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, (E)-tert-butyl 4-(1-amino-3-ethoxy-3-oxoprop-1-enyl)piperidine-1-carboxylate serves as a building block for the synthesis of more complex organic molecules. Its unique structure allows it to be a valuable component in creating a variety of organic compounds for different applications.
Used in Medicinal Chemistry:
(E)-tert-butyl 4-(1-amino-3-ethoxy-3-oxoprop-1-enyl)piperidine-1-carboxylate is used as a starting material in medicinal chemistry for the design and synthesis of potential drug candidates. Its structural features may offer new avenues for the development of therapeutic agents targeting specific biological pathways or receptors.
Used in Drug Discovery:
In the drug discovery process, (E)-tert-butyl 4-(1-amino-3-ethoxy-3-oxoprop-1-enyl)piperidine-1-carboxylate is utilized as a compound of interest for screening and optimization. Its potential biological activity and chemical properties make it a promising candidate for further investigation and development into effective pharmaceuticals.
Used in Chemical Biology:
(E)-tert-butyl 4-(1-amino-3-ethoxy-3-oxoprop-1-enyl)piperidine-1-carboxylate is employed in chemical biology research to study the interactions between small molecules and biological targets. Understanding these interactions can provide insights into the compound's potential uses and mechanisms of action in biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 521302-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,1,3,0 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 521302-69:
(8*5)+(7*2)+(6*1)+(5*3)+(4*0)+(3*2)+(2*6)+(1*9)=102
102 % 10 = 2
So 521302-69-2 is a valid CAS Registry Number.
521302-69-2Relevant articles and documents
The Bohlmann-Rahtz route to functionalised pyridine scaffolds and their use in library synthesis
Bashford, Katherine E.,Burton, Matthew B.,Cameron, Stuart,Cooper, Anthony L.,Hogg, Rebecca D.,Kane, Peter D.,MacManus, David A.,Matrunola, Christopher A.,Moody, Christopher J.,Robertson, Avril A. B.,Warne, Mark R.
, p. 1627 - 1629 (2003)
The Bohlmann-Rahtz reaction has been used to prepare 2,3,6-trisubstituted pyridines suitable for use in library synthesis. The synthesis of piperidine substituted nicotinic acid derivative 9 has been optimised and carried out on a large scale to give ca. 500 g of scaffold which was used in the generation of the pyridine library 11.
