219560-29-9 Usage
Uses
Used in Pharmaceutical Industry:
(S)-N-benzyloxycarbonyl-homo-β-proline is used as a chiral building block for the synthesis of biologically active molecules due to its unique structural properties. This makes it a crucial component in the development of new pharmaceutical compounds.
Used in Medicinal Chemistry:
(S)-N-benzyloxycarbonyl-homo-β-proline is used as a precursor in the production of peptide and peptidomimetic compounds. Its role in the creation of these compounds aids in the advancement of medicinal chemistry, as these compounds can have various therapeutic applications.
Used in Drug Discovery:
(S)-N-benzyloxycarbonyl-homo-β-proline's ability to act as a chiral building block also makes it a valuable tool in drug discovery. Researchers can use (S)-N-benzyloxycarbonyl-homo-β-proline to create novel molecular structures with potential therapeutic effects, contributing to the development of new drugs and treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 219560-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,5,6 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 219560-29:
(8*2)+(7*1)+(6*9)+(5*5)+(4*6)+(3*0)+(2*2)+(1*9)=139
139 % 10 = 9
So 219560-29-9 is a valid CAS Registry Number.
219560-29-9Relevant academic research and scientific papers
Chiral bicyclic guanidine as a versatile bronsted base catalyst for the enantioselective michael reactions of dithiomalonates and β-keto thioesters
Ye, Weiping,Jiang, Zhiyong,Zhao, Yujun,Goh, Serena Li Min,Leow, Dasheng,Soh, Ying-Teck,Tan, Choon-Hong
, p. 2454 - 2458 (2008/09/19)
A chiral bicyclic guanidine was developed as a versatile Bronsted base catalyst for the enantioselective Michael reactions of dithiomalonates and β-keto thioesters using a range of acceptors including maleimides, cyclic enones, furanone and acyclic 1,4-di
Conformationally constrained no synthase inhibitors: Rigid analogs of L- N-iminoethylornithine
Eustache, Jacques,Grob, Alfred,Lam, Charles,Sellier, Odile,Schulz, Gerhard
, p. 2961 - 2966 (2007/10/03)
The synthesis of eight rigid analogs of L-N-iminoethylomithine (L-NIO) is described. The compounds have been evaluated for their inhibition of inducible nitric oxide synthase. Preliminary structure-activity relationships are discussed.
