824943-40-0 Usage
Uses
Used in Pharmaceutical Industry:
(2S,5R)-5-HYDROXYPIPECOLIC ACID HCL is used as a precursor in drug development for its potential to contribute to the synthesis of pharmaceuticals with specific biological activities. Its unique stereochemistry allows for targeted interactions with biological molecules, enhancing the efficacy of resulting drugs.
Used in Organic Synthesis:
In the field of organic synthesis, (2S,5R)-5-HYDROXYPIPECOLIC ACID HCL serves as a key intermediate compound for the creation of complex organic molecules. Its versatility in chemical reactions facilitates the production of a wide range of bioactive compounds for research and commercial applications.
Used in Research:
(2S,5R)-5-HYDROXYPIPECOLIC ACID HCL is utilized in scientific research to study the effects of stereochemistry on biological activity. Understanding how (2S,5R)-5-HYDROXYPIPECOLIC ACID HCL interacts with other molecules can provide insights into the development of more effective drugs and therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 824943-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,4,9,4 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 824943-40:
(8*8)+(7*2)+(6*4)+(5*9)+(4*4)+(3*3)+(2*4)+(1*0)=180
180 % 10 = 0
So 824943-40-0 is a valid CAS Registry Number.
824943-40-0Relevant academic research and scientific papers
Diastereoselective synthesis of (2Ss,5R)-5-hydroxypipecolic acid and 6-substituted derivatives
Botman, Peter N. M.,Dommerholt, F. Jan,De Gelder, Rene,Broxterman, Quirinus B.,Schoemaker, Hans E.,Rutjes, Floris P. J. T.,Blaauw, Richard H.
, p. 4941 - 4944 (2007/10/03)
(Chemical Equation Presented) Herein, we report a diastereoselective synthesis of the natural product (2S,5R)-5-hydroxypipecolic acid and 6-substituted derivatives thereof. The key step in the synthetic sequence is a novel highly diastereoselective epoxidation reaction of an enantiomerically pure cyclic enamide intermediate.
