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L-Phenylalanine, N-[1-[(phenylmethoxy)carbonyl]-L-prolyl]-, 1,1-dimethylethyl ester is a complex organic compound with the chemical formula C23H27N2O5. It is a derivative of the amino acid L-phenylalanine, featuring a proline residue attached to the phenylalanine through a phenylmethoxycarbonyl linker. The compound is further modified with a 1,1-dimethylethyl (tert-butyl) ester group, which is a bulky, non-polar group that can protect the carboxylic acid functionality. This specific chemical structure is often found in peptide chemistry, where it may be used to protect certain functional groups during synthesis, or in the development of pharmaceuticals, where such structures can influence the properties of peptide drugs, such as their stability, solubility, or bioavailability. The compound's exact role and application can vary widely depending on the context in which it is used, but it generally represents a sophisticated building block in the field of organic synthesis and medicinal chemistry.

2090-57-5

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2090-57-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2090-57-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,9 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2090-57:
(6*2)+(5*0)+(4*9)+(3*0)+(2*5)+(1*7)=65
65 % 10 = 5
So 2090-57-5 is a valid CAS Registry Number.

2090-57-5Downstream Products

2090-57-5Relevant academic research and scientific papers

STUDIES ON AMINO ACIDS AND PEPTIDES-III. 2,4-BIS(4-METHOXYPHENYL)-1,3,2,4-DITHIADIPHOSPHETANE 2,4-DISULFIDE, LR, AS A NEW RACEMIZATION FREE COUPLING REAGENT IN PEPTIDE SYNTHESIS

Pedersen, U.,Thorsen, M.,El-Khrisy, E. -E. A. M.,Clausen, K.,Lawesson, S. -O.

, p. 3267 - 3269 (1982)

The easily accesable 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane 2,4-disulfide, LR, has been reacted with salts of N-protected amino acids 1 (Z-Gly-OH, Boc-Gly-OH, Boc-S-Ser(Bzl)-OH, Bos-S-Tyr(Bzl)-OH, Z-S-Arg(Z2)-OH, and Z-S-Pro-OH), at room tem

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