359586-68-8 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
(1S,2S)-2-((S)-1-phenylethylaMino)cyclopentanecarboxylic acid hydrochloride is utilized as a chiral building block for the synthesis of biologically active molecules. Its unique structure allows for the creation of new compounds with potential therapeutic properties, contributing to the advancement of medicine.
Used in the Synthesis of Potential Drug Candidates:
In the pharmaceutical industry, (1S,2S)-2-((S)-1-phenylethylaMino)cyclopentanecarboxylic acid hydrochloride is used as a precursor in the development of new drug candidates. Its versatility in chemical reactions enables the exploration of various therapeutic avenues, potentially leading to the discovery of treatments for a range of medical conditions.
Used in the Study of Chiral Chemistry:
(1S,2S)-2-((S)-1-phenylethylaMino)cyclopentanecarboxylic acid hydrochloride is employed in the study of chiral chemistry to understand the role of stereochemistry in biological activity. This knowledge is crucial for the design of more effective and selective drugs, minimizing side effects and improving patient outcomes.
Check Digit Verification of cas no
The CAS Registry Mumber 359586-68-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,9,5,8 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 359586-68:
(8*3)+(7*5)+(6*9)+(5*5)+(4*8)+(3*6)+(2*6)+(1*8)=208
208 % 10 = 8
So 359586-68-8 is a valid CAS Registry Number.
359586-68-8Relevant academic research and scientific papers
(S,S)-trans-cyclopentane-constrained peptide nucleic acids. A general backbone modification that improves binding affinity and sequence specificity
Pokorski, Jonathan K.,Witschi, Mark A.,Purnell, Bethany L.,Appella, Daniel H.
, p. 15067 - 15073 (2007/10/03)
Replacing the ethylenediamine portion of aminoethylglycine peptide nucleic acids (aegPNAs) with one or more (S,S)-trans-cyclopentane diamine units significantly increases binding affinity and sequence specificity to complementary DNA, making these modifie
