183070-41-9 Usage
Uses
Used in Pharmaceutical Industry:
(S)-Benzyl 2-(benzyloxycarbonylamino)-3-(4-(trifluoromethylsulfonyloxy)phenyl)propanoate is used as a potential pharmaceutical compound for its possible biological activity due to the presence of various functional groups that may interact with biological systems.
Used in Chemical Research:
(S)-Benzyl 2-(benzyloxycarbonylamino)-3-(4-(trifluoromethylsulfonyloxy)phenyl)propanoate is used as a subject of study in chemical research to explore its reactivity, properties, and potential applications in the synthesis of other complex molecules or as a precursor in organic synthesis.
Used in Material Science:
(S)-Benzyl 2-(benzyloxycarbonylamino)-3-(4-(trifluoromethylsulfonyloxy)phenyl)propanoate may be used in material science for the development of new materials with unique properties, such as those with enhanced chemical stability or specific interactions with other molecules,得益于其复杂的化学结构和多样的官能团。(Translation: Benefiting from its complex chemical structure and diverse functional groups.)
Check Digit Verification of cas no
The CAS Registry Mumber 183070-41-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,0,7 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 183070-41:
(8*1)+(7*8)+(6*3)+(5*0)+(4*7)+(3*0)+(2*4)+(1*1)=119
119 % 10 = 9
So 183070-41-9 is a valid CAS Registry Number.
183070-41-9Relevant academic research and scientific papers
Stereospecific synthesis of 4-carboxyphenylalanine and derivatives for use in Fmoc-based solid-phase peptide synthesis
Wang, Wei,Obeyesekere, Nihal U.,McMurray, John S.
, p. 6661 - 6664 (2007/10/03)
Starting from N(α)-benzyloxycarbonyl-L-tyrosine(O-triflate) benzyl ester, we have prepared enantiomerically pure 4-carboxyphenylalanine and 4-methoxycarbonylphenylalanine derivatives using palladium (0) catalyzed carbonylation reactions. These unnatural amino acids were suitably protected and were used in solid-phase peptide synthesis using the Fmoc/t-butyl approach.
Synthesis of novel L-phenylalanine derivatives substituted with a keto ylide as stable precursor of a vicinal tricarbonyl moiety
Fretz, Heinz
, p. 8475 - 8478 (2007/10/03)
Novel L-phenylalanine derivatives 5 containing a vicinal tricarbonyl moiety at the para position of the phenyl ring were prepared in 4 steps starting from N(α)-Cbz-L-tyrosine benzyl ester. A 7 step reaction sequence lead to N(α)-Fmoc protected derivatives 9 with the tricarbonyl structure masked as its stable keto ylide precursor, which is suitable for solid phase peptide synthesis. The phosphoranylidene intermediates 8 were transformed to the trioxo compounds 5 with Oxone as oxidant.
