1273577-31-3 Usage
Description
(2S,4S,5R)-tert-butyl 5-ethyl-2-(2-hydroxyethyl)piperidine-4-carboxylate is a chiral chemical compound with the molecular formula C16H31NO3. It is a tert-butyl ester derivative of a piperidine carboxylic acid, featuring an ethyl group and a hydroxyethyl group. (2S,4S,5R)-tert-butyl 5-ethyl-2-(2-hydroxyethyl)piperidine-4-carboxylate is characterized by its specific stereochemistry at the 2nd, 4th, and 5th positions, making it a versatile building block in the synthesis of pharmaceuticals and other organic compounds. Its structure and functional groups contribute to its potential application in medicinal chemistry.
Uses
Used in Pharmaceutical Synthesis:
(2S,4S,5R)-tert-butyl 5-ethyl-2-(2-hydroxyethyl)piperidine-4-carboxylate is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into complex molecular structures, enhancing the development of new drugs with specific therapeutic properties.
Used in Organic Chemistry:
In the field of organic chemistry, (2S,4S,5R)-tert-butyl 5-ethyl-2-(2-hydroxyethyl)piperidine-4-carboxylate serves as a valuable precursor for the creation of new chemical entities. Its unique structure allows for the exploration of novel chemical reactions and the generation of compounds with diverse properties and potential applications.
Used in Medicinal Chemistry:
(2S,4S,5R)-tert-butyl 5-ethyl-2-(2-hydroxyethyl)piperidine-4-carboxylate is utilized as a chiral building block in medicinal chemistry, where its stereochemistry plays a crucial role in the biological activity of the resulting compounds. This makes it an important component in the design and synthesis of enantiomerically pure drugs with targeted therapeutic effects.
Used in Research and Development:
In research and development, (2S,4S,5R)-tert-butyl 5-ethyl-2-(2-hydroethyl)piperidine-4-carboxylate is employed as a model compound to study the effects of stereochemistry on chemical reactivity and biological activity. Its use aids in understanding the fundamental principles of stereoselective synthesis and the development of innovative synthetic routes to enantiomerically pure compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1273577-31-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,3,5,7 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1273577-31:
(9*1)+(8*2)+(7*7)+(6*3)+(5*5)+(4*7)+(3*7)+(2*3)+(1*1)=173
173 % 10 = 3
So 1273577-31-3 is a valid CAS Registry Number.
