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Z-(S-benzyl)-Cys-(sulfoxide)-OH is a chemical compound that belongs to the class of sulfoxides, which are derivatives of sulfur-containing amino acids. This specific compound features a cysteine residue with a benzyl group attached to the sulfur atom, forming an S-benzyl cysteine. The sulfoxide group is present, indicating an oxidation state of the sulfur atom. It is often used in peptide synthesis and as a building block for more complex organic molecules, particularly in the pharmaceutical and chemical industries. The compound's structure and properties make it a valuable intermediate in the synthesis of various biologically active peptides and other sulfur-containing compounds.

73243-11-5

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73243-11-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73243-11-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,4 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 73243-11:
(7*7)+(6*3)+(5*2)+(4*4)+(3*3)+(2*1)+(1*1)=105
105 % 10 = 5
So 73243-11-5 is a valid CAS Registry Number.

73243-11-5Downstream Products

73243-11-5Relevant academic research and scientific papers

L-METHIONINE OXIDATION: NOVEL AND UNANTICIPATED TRANSFORMATIONS WITH 4-tBUTYL IODOXYBENZENE

Ranganathan, S.,Ranganathan, D.,Singh, S.K.,Bhattacharyya, D.,Shanthy, S.,Singh, G.P.

, p. 5363 - 5366 (2007/10/02)

4-tButyl iodoxybenzene transforms Bz-Met-OMe to products arising from, S oxidation and C-H insertion followed by degradation.Z-Met(sulfoxide)-OMe is very effective in bringing about ester hydrolysis via intramolecular attack.The S oxidation to sulfoxides and then to sulfones can be monitored and controlled, proceeds with chiral retention, affects neither the peptide bond nor the protecting groups and has been further illustrated with,Z-Gly-Met-OMe, Z-Met-OMe and Z-S(benzyl)-Cys-OMe.

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