183070-41-9 Usage
General Description
"(S)-Benzyl 2-(benzyloxycarbonylamino)-3-(4-(trifluoromethylsulfonyloxy)phenyl)propanoate" is a complex organic chemical compound possessing several functional groups including sulfone, benzyloxycarbonyl, and ester groups. The benzyl group is a common phenyl group attached to a CH2, and the benzyloxycarbonylamino refers to the carboxamide group linked to a benzyl group. The trifluoromethylsulfonyloxy group contains fluorine, sulfur and oxygen atoms, which could lend the molecule possible biological activity. As a derivative of propanoic acid, it also contains a carboxylate ester at its terminal. However, without more information, the specific properties, reactivity, and applications of this compound are not clear.
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 articles and documents
A concise synthesis of enantiomerically pure L-(4-Boronophenyl)alanine from L-tyrosine
Nakamura, Hiroyuki,Fujiwara, Masaru,Yamamoto, Yoshinori
, p. 7529 - 7530 (1998)
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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.