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N-(benzyloxycarbonyl)-L-leucyl-L-tyrosine methyl ester is a complex organic compound that belongs to the class of dipeptides, which are short chains of amino acids. This specific compound is composed of two amino acids, L-leucine and L-tyrosine, linked together by a peptide bond. The N-terminus of the compound is protected by a benzyloxycarbonyl (Z) group, which is a common protecting group used in peptide synthesis to prevent unwanted side reactions. The C-terminus is modified with a methyl ester group, which can be used to facilitate the solubility of the compound in certain solvents or to protect the carboxyl group during synthesis. N-(benzyloxycarbonyl)-L-leucyl-L-tyrosine methyl ester is often used in the field of peptide chemistry for the synthesis of larger peptides and proteins, as well as in the development of pharmaceuticals and bioactive molecules.

2541-25-5

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2541-25-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2541-25-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,4 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2541-25:
(6*2)+(5*5)+(4*4)+(3*1)+(2*2)+(1*5)=65
65 % 10 = 5
So 2541-25-5 is a valid CAS Registry Number.

2541-25-5Relevant academic research and scientific papers

Studies on the Synthesis of Aryl Ethers Using Arene-Manganese Chemistry

Pearson, Anthony J.,Bruhn, Paul R.

, p. 7092 - 7097 (2007/10/02)

Selective arylation of polyfunctional phenols, using chlorobenzene- and p-chlorotoluene-manganese tricarbonyl cations, is described.The intermediate arene-manganese complexes are found to undergo stereo- and regioselective reactions with Schoellkopf's chiral glycine enolate equivalent to give dienyl-Mn(CO)3 complexes.Treatment of these complexes with N-bromosuccinimide at room temperature, followed by hydrolysis of the dihydropyrazine, gives diaryl ethers in which one of the aromatic rings is an arylglycine methyl ester.

Peptide Synthesis by Means of Immobilized Enzymes. I. Immobilized α-Chimotripsin

Koennecke, Andreas,Bullerjahn, Ralf,Jakubke, Hans-Dieter

, p. 469 - 482 (2007/10/02)

α-Chymotrypsin covalently bound to silica, enzacryl AA, and enzacryl AH catalyzes peptide bond formation between N-protected dipeptide methyl esters and H-Leu-NH2 with results similar to those with the free enzyme.The influence of water-miscible and water

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