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N-benzoyl-L-cystine ethyl ester is a chemical compound with the molecular formula C15H19NO4S. It is a derivative of the amino acid cysteine, where the cysteine molecule is modified by the addition of a benzoyl group (C6H5CO-) to the nitrogen atom and an ethyl ester group (CH3CH2O-) to the carboxylic acid group. N-benzoyl-L-cystine ethyl ester is often used in peptide synthesis and as a building block for the creation of more complex molecules. It is also known for its potential applications in the pharmaceutical industry, particularly in the development of drugs that target specific biological pathways. The compound's structure allows for the formation of disulfide bonds, which are crucial for the stability and function of many proteins.

3842-34-0

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3842-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3842-34-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,4 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3842-34:
(6*3)+(5*8)+(4*4)+(3*2)+(2*3)+(1*4)=90
90 % 10 = 0
So 3842-34-0 is a valid CAS Registry Number.

3842-34-0Relevant academic research and scientific papers

NO-mediated aromatic nitration during decomposition of phenolic S-nitrosothiols in non-aqueous aerobic medium

Petit,Bernardes-Genisson,Hoffmann,Souchard,Labidalle

, p. 1634 - 1638 (2007/10/03)

Five novel S-nitrosothiol compounds (6-10) derived from L-cysteine were generated in solution and their decomposition rate was followed by UV spectroscopy. In acetonitrile, compounds 9 and 10 were the most stable of this series with a half-life of 24 h. T

Coordination of cysteine and hisyidine derivatives to the pyrazolylborate-zinc unit

Ruf, Michael,Burth, Rainer,Weis, Karl,Vahrenkamp, Heinrich

, p. 1251 - 1257 (2007/10/03)

Highly substituted pyrazolylborate ligands TpR,Me were used to limit the coordination number of zinc towards cysteine-and histidine-derived coligands. Monodentate thiolate attachment (→ 1a-f) was achieved with N- and C-protected cysteine, monodentate carboxylate attachment (→ 3) with N-protected histidine. C-protected cysteine was found to form a five-membered N,S-chelate ring (2). While imidazole coordination with N- and C-protected histidine could not be achieved, cationic pyrazolylborate-zinc-collgand complexes [TpZn-L]+ (4a, b) were obtained for L = 2-methylimidazole. The new complexes were characterized by their spectra and three structure determinations. VCH Verlagsgesellschaft mbH 1996.

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