660862-78-2 Usage
Uses
Used in Organic Synthesis:
(R)-3-(allyloxy)-2-(tert-butoxycarbonylamino)propanoic acid is used as a building block for the synthesis of more complex organic molecules. Its unique functional groups, such as the allyloxy and tert-butoxycarbonylamino moieties, can be utilized in various chemical reactions to create a wide range of compounds with different properties and applications.
Used in Pharmaceutical Industry:
(R)-3-(allyloxy)-2-(tert-butoxycarbonylamino)propanoic acid is used as an intermediate in the development of new pharmaceutical compounds. Its chiral nature and functional groups make it a promising candidate for the synthesis of enantiomerically pure drugs, which can have improved efficacy and reduced side effects compared to their racemic counterparts.
Used in Materials Science:
(R)-3-(allyloxy)-2-(tert-butoxycarbonylamino)propanoic acid may be employed in the development of novel materials with specific properties. Its chemical structure could be exploited to create materials with tailored characteristics, such as improved mechanical strength, thermal stability, or biocompatibility, depending on the desired application.
Check Digit Verification of cas no
The CAS Registry Mumber 660862-78-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,0,8,6 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 660862-78:
(8*6)+(7*6)+(6*0)+(5*8)+(4*6)+(3*2)+(2*7)+(1*8)=182
182 % 10 = 2
So 660862-78-2 is a valid CAS Registry Number.
660862-78-2Relevant academic research and scientific papers
Demizu, Yosuke,Yamagata, Nanako,Nagoya, Saori,Sato, Yukiko,Doi, Mitsunobu,Tanaka, Masakazu,Nagasawa, Kazuo,Okuda, Haruhiro,Kurihara, Masaaki
, p. 6155 - 6165 (2011)
Stapled helical l-leucine-based heptapeptides were synthesized and used as catalysts for the enantioselective epoxidation of α,β-unsaturated ketones. All N-terminal free stapled peptides were successfully used as chiral catalysts. Among them, the use of H-hS3,7hS-10 gave epoxide products with high enantioselectivities of up to 99% ee. Furthermore, the dominant conformations of the N-terminal protected stapled peptides R 3,7R-10 and hS3,7hS-10 were investigated by 1H NMR, IR, CD spectra, and X-ray crystallographic analysis. The peptide R3,7R-10 formed a right-handed (P) α-helix in solution and in the crystalline state, while hS 3,7hS-10 formed a right-handed (P) 310-helix in solution.
