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The chemical compound "C46H66N14O12S2" is a complex organic molecule with a molecular formula indicating the presence of 46 carbon atoms, 66 hydrogen atoms, 14 nitrogen atoms, 12 oxygen atoms, and 2 sulfur atoms. C46H66N14O12S2 is likely a peptide or protein, given the high nitrogen content, which is characteristic of amino acids, the building blocks of proteins. The presence of sulfur atoms suggests that it may contain cysteine or methionine, amino acids that are known for their sulfur-containing side chains. The compound's structure and function would be determined by the specific arrangement of these amino acids and the chemical bonds between them. The molecular weight can be calculated based on the atomic masses of the constituent elements, providing further insight into its properties.

6752-21-2

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6752-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6752-21-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,5 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6752-21:
(6*6)+(5*7)+(4*5)+(3*2)+(2*2)+(1*1)=102
102 % 10 = 2
So 6752-21-2 is a valid CAS Registry Number.

6752-21-2Upstream product

6752-21-2Downstream Products

6752-21-2Relevant academic research and scientific papers

The use of hydrogen peroxide for closing disulfide bridges in peptides

Sidorova,Molokoedov,Az'muko,Kudryavtseva,Krause,Ovchinnikov,Bespalova

, p. 101 - 110 (2004)

The use of hydrogen peroxide for the formation of disulfide bridges was studied in 15 peptides of various lengths and structures. The oxidation of peptide thiols by hydrogen peroxide was shown to proceed under mild conditions without noticeable side reactions of Trp, Tyr, and Met residues. Yields of the corresponding cyclic disulfides were high and mostly exceeded those obtained with other oxidative agents, in particular, iodine. It was established that the use of hydrogen peroxide in organic medium also provided sufficiently high yields when large-scale syntheses of oxytocin and octreotide (up to 10 g) were carried out.

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