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Glycine, N-[N-[(phenylmethoxy)carbonyl]-L-tryptophyl]-, ethyl ester is a complex organic compound with the chemical formula C26H28N2O5. It is a derivative of glycine, an amino acid, and L-tryptophan, another essential amino acid. The compound features a phenylmethoxycarbonyl group attached to the L-tryptophan moiety, which is then connected to the glycine unit through an amide bond. The ethyl ester group is present at the carboxylic acid end of the glycine, making it a protected form of the dipeptide. Glycine, N-[N-[(phenylmethoxy)carbonyl]-L-tryptophyl]-, ethyl ester is significant in peptide chemistry, as it can be used as a building block for the synthesis of larger peptides and proteins, with the protecting group facilitating controlled coupling reactions. The ethyl ester can be removed under specific conditions to yield the free carboxylic acid, allowing for further peptide bond formation.

2891-15-8

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2891-15-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2891-15-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,9 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2891-15:
(6*2)+(5*8)+(4*9)+(3*1)+(2*1)+(1*5)=98
98 % 10 = 8
So 2891-15-8 is a valid CAS Registry Number.

2891-15-8Relevant academic research and scientific papers

Phosphine-based redox catalysis in the direct traceless staudinger ligation of carboxylic acids and azides

Kosal, Andrew D.,Wilson, Erin E.,Ashfeld, Brandon L.

supporting information, p. 12036 - 12040 (2013/01/16)

Redox catalysis: Aryl amides, imides, lactams, and dipeptides are obtained through a direct Staudinger ligation mediated by phosphine-based redox catalysis (see scheme). Mechanistic studies indicate the involvement of a phosphonium carboxylate intermediate that leads to a 1,3-acyl migration and thus results in C-N bond formation. Copyright

Metal-free direct amidation of peptidyl thiol esters with α-amino acid esters

Chen, Hao,He, Maomao,Wang, Yaya,Zhai, Linhui,Cui, Yongbo,Li, Yangyan,Lee, Yan,Zhou, Haibing,Hong, Xuechuan,Deng, Zixin

supporting information; experimental part, p. 2723 - 2726 (2011/11/06)

Metal-free direct amidation of peptidyl thiol esters with α-amino acid esters in the presence of bis(trimethylsilyl) acetamide (BSA) has been developed. This general method provides convenient access to N-protected peptides in good yields under mild condi

2-PHENOXY- AND 2-PHENYLSULFOMAMIDE DERIVATIVES WITH CCR3 ANTAGONISTIC ACTIVITY FOR THE TREATMENT OF ASTHMA AND OTHER INFLAMMATORY OR IMMUNOLOGICAL DISORDERS

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Page/Page column 43-44, (2008/06/13)

The present invention relates to a benzenesulfonamide derivative of formula (I), which is useful as an active ingredient of pharmaceutical preparations. The benzenesulfonamide derivatives of the present invention have CCR3 (CC type chemokine receptor) ant

A New Route toward 4-Substituted Pyrazino[2,1-b]quinazoline-3,6-dione Systems. Total Synthesis of Glyantrypine

Cledera, Pilar,Avendano, Carmen,Carlos Menendez

, p. 1743 - 1749 (2007/10/03)

Treatment of sodium N-(o-azidobenzoyl)aminoacylglycinates 8 with acetic anhydride afforded 1-acetyl-4-(o-azidobenzoyl)-2,5-piperazinediones 7, with complete retention of the stereochemistry. The intramolecular aza Wittig reactions of compounds 7 in the pr

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