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((2R)-2-benzyloxycarbonylamino-4-methyl-pentanoylamino)acetic acid ethyl ester is a complex organic compound with the molecular formula C20H29NO5. It is a derivative of amino acids, featuring a benzyloxycarbonyl (Cbz) protecting group and an ethyl ester moiety. ((2R)-2-benzyloxycarbonylamino-4-methyl-pentanoylamino)acetic acid ethyl ester is significant in peptide synthesis, where the Cbz group is used to protect the amino group during the assembly of peptide chains, preventing unwanted side reactions. The ethyl ester group is a common ester functionality that can be hydrolyzed under acidic or basic conditions, which is useful for the controlled release of the peptide in biological systems. The chiral center at the 2-position (2R) indicates that the molecule has a specific three-dimensional arrangement, which is crucial for its biological activity and reactivity. ((2R)-2-benzyloxycarbonylamino-4-methyl-pentanoylamino)acetic acid ethyl ester is a valuable intermediate in the synthesis of various peptides and pharmaceuticals, highlighting its importance in the field of medicinal chemistry.

79171-66-7

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79171-66-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79171-66-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,1,7 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79171-66:
(7*7)+(6*9)+(5*1)+(4*7)+(3*1)+(2*6)+(1*6)=157
157 % 10 = 7
So 79171-66-7 is a valid CAS Registry Number.

79171-66-7Downstream Products

79171-66-7Relevant academic research and scientific papers

Circular dichroism studies on absolute configuration assignment of peptidomimetics with a terminal chiral 3-arylpropionic acid unit

Frelek, Jadwiga,Fryszkowska, Anna,Kwit, Marcin,Ostaszewski, Ryszard

, p. 2469 - 2478 (2006)

The relationship between the molecular structure of peptidomimetics 1 and their chiroptical properties has been studied using circular dichroism spectroscopy. It was demonstrated that the sign of the Cotton effects occurring around 230 and 270 nm enables the direct assignment of stereochemistry at C-1 and C-3 carbon atoms. The TD-DFT calculations of the circular dichroism (CD) spectrum of one of the model compounds confirm the absolute stereochemistry assignment made experimentally. Thus, CD spectroscopy proved to be a simple, reliable and general tool for the determination of the absolute configuration of the stereogenic centers of peptidomimetics with a terminal 3-arylpropionic group.

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