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(S)-4-benzyloxycarbonylamino-2-oxazolidone is a chiral compound with the molecular formula C10H10N2O4. It is a derivative of 2-oxazolidone, featuring a benzyloxycarbonyl (Cbz) protecting group attached to the 4-position and an amino group at the 4-position as well. This chemical is significant in organic synthesis, particularly in peptide chemistry, where it serves as a building block for the synthesis of peptides and other biologically active molecules. The (S)-configuration indicates that the compound has a specific three-dimensional arrangement of atoms, which is crucial for its reactivity and potential applications in asymmetric synthesis. The benzyloxycarbonyl group is a common protecting group used to shield the amino group from unwanted reactions until it is deprotected at a later stage in the synthesis process.

7705-88-6

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7705-88-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7705-88-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,0 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7705-88:
(6*7)+(5*7)+(4*0)+(3*5)+(2*8)+(1*8)=116
116 % 10 = 6
So 7705-88-6 is a valid CAS Registry Number.

7705-88-6Relevant academic research and scientific papers

(R)-tert-butoxycarbonylamino-fluorenylmethoxycarbonyl-glycine from (S)-benzyloxycarbonyl-serine or from papain resolution of the corresponding amide or methyl ester

Sypniewski, Michal,Penke, Botond,Simon, Lajos,Rivier, Jean

, p. 6595 - 6600 (2007/10/03)

The enantiospecific synthesis of (R)-Boc-(Fmoc)-aminoglycine 7 was achieved. (S)-Cbz-serine 1 was reacted with diphenylphosphoryl azide in the presence of triethylamine to yield cyclic(S) carbamate 2. The ring nitrogen of 2 was protected with a Boc group.

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