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S-phenyl (2S)-2-{[(benzyloxy)carbonyl]amino}-3-phenylpropanethioate is a complex organic compound with the molecular formula C26H25NO3S. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it belongs to the class of compounds known as thiol esters. This specific compound features a phenyl group attached to a sulfur atom, which is in turn connected to a propanedithioate backbone. The molecule also includes a benzyloxycarbonyl group, which serves as a protecting group in organic synthesis, and an amino group. S-phenyl (2S)-2-{[(benzyloxy)carbonyl]amino}-3-phenylpropanethioate is typically used as an intermediate in the synthesis of pharmaceuticals and other organic compounds, where its reactivity and the presence of functional groups can be exploited for further chemical transformations.

2075-55-0

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2075-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2075-55-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,7 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2075-55:
(6*2)+(5*0)+(4*7)+(3*5)+(2*5)+(1*5)=70
70 % 10 = 0
So 2075-55-0 is a valid CAS Registry Number.

2075-55-0Relevant academic research and scientific papers

Real-time colorimetric screening of endopeptidase inhibitors using adenosine triphosphate (ATP)-stabilized gold nanoparticles

Kim, Mi Hee,Lee, Soo Suk,Chung, Sang J.,Jang, Hyun Hye,Yi, Sujung,Kim, Sudeok,Chang, Suk-Kyu,Han, Min Su

, p. 2228 - 2231 (2010)

The gold nanoparticles (AuNPs) that were stabilized with adenosine triphosphate (ATP) were stable over a wide range of pHs for the buffer, even in the presence of high concentrations of salt and protein. However, these stabilized AuNPs immediately aggrega

Decarbonylative approach to the synthesis of enamides from amino acids: Stereoselective synthesis of the (Z)-aminovinyl-d-cysteine unit of mersacidin

Garcia-Reynaga, Pablo,Carrillo, Angela K.,Vannieuwenhze, Michael S.

supporting information; experimental part, p. 1030 - 1033 (2012/04/04)

The Pd- and Ni-promoted decarbonylation of amino acid thioesters proceeds smoothly to yield enamides. The synthesis of the (S)-(Z)-AviMeCys subunit of mersacidin, an MRSA-active lantibiotic, via this approach, is described.

Ambient temperature synthesis of high enantiopurity N-protected peptidyl ketones by peptidyl thiol ester-boronic acid cross-coupling

Yang, Hao,Li, Hao,Wittenberg, Ruediger,Egi, Masahiro,Huang, Wenwei,Liebeskind, Lanny S.

, p. 1132 - 1140 (2007/10/03)

α-Amino acid thiol esters derived from N-protected mono-, di-, and tripeptides couple with aryl, π-electron-rich heteroaryl, or alkenyl boronic acids in the presence of stoichiometric Cu(I) thiophene-2-carboxylate and catalytic Pd2(dba)3/triethylphosphite to generate the corresponding N-protected peptidyl ketones in good-to-excellent yields and in high enantiopurity. Triethylphosphite plays a key role as a supporting ligand by mitigating an undesired palladium-catalyzed decarbonylation-β-elimination of the α-amino thiol esters. The peptidyl ketone synthesis proceeds at room temperature under nonbasic conditions and demonstrates a high tolerance to functionality.

A new convenient preparation of thiol esters utilizing N-acylbenzotriazoles

Katritzky, Alan R.,Shestopalov, Aleksandr A.,Suzuki, Kazuyuki

, p. 1806 - 1813 (2007/10/03)

Diverse thiol esters were synthesized in good to excellent yields (76-99%) by reactions of thiophenol, benzyl mercaptan, ethyl mercaptoacetate, and mercaptoacetic acid with N-acylbenzotriazoles under mild conditions. These results demonstrate the utility of N-acylbenzotriazoles as mild S-acylating agents, especially when the corresponding acid chlorides are not readily available.

Fluorometric Assay Protocol for Protease-Catalyzed Transesterification Reactions in Organic Solvents

Han, Min Su,Jung, Sang Oh,Kim, Mahn-Joo,Kim, Dong H.

, p. 2853 - 2855 (2007/10/03)

A flourometric assay protocol for a subtilisin-catalyzed transesterification reaction in n-hexane has been developed. The method makes use of a Michael acceptor that forms a fluorescent adduct with thiophenol, one of the products generated in the transest

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