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Tr-Trp(Mbs)-OBzl, also known as Nα-(9-fluorenylmethoxycarbonyl)-Nε-trityl-L-tryptophan, is a synthetic peptide building block used in solid-phase peptide synthesis. It features a tryptophan residue with a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group on the α-amino group and a trityl (Trt) protecting group on the ε-amino group. The benzyl (OBzl) group is attached to the indole nitrogen of the tryptophan, which is crucial for protecting the side chain during peptide synthesis. This chemical is essential for the stepwise assembly of peptides and proteins, as it allows for the controlled addition of amino acids in a specific sequence while maintaining the integrity of the growing peptide chain.

83595-60-2

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83595-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83595-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,9 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83595-60:
(7*8)+(6*3)+(5*5)+(4*9)+(3*5)+(2*6)+(1*0)=162
162 % 10 = 2
So 83595-60-2 is a valid CAS Registry Number.

83595-60-2Relevant academic research and scientific papers

New Protecting Groups for the Indole Ring of Tryptophan in Peptide Synthesis: 2,4,6-Trimethoxybenzenesulfonyl and 4-Methoxy-2,3,6-trimethylbenzenesulfonyl Groups

Fukuda, Tsunehiko,Wakimasu, Mitsuhiro,Kobayashi, Shigeru,Fujino, Masahiko

, p. 2825 - 2835 (2007/10/02)

Five substituted benzenesulfonyl groups, p-toluenesulfonyl, p-methoxybenzenesulfonyl, 2,4-dimethoxybenzenesulfonyl, 2,4,6-trimethoxybenzenesulfonyl, and 4-methoxy-2,3,6-trimethylbenzenesulfonyl, were introduced at Nin of tryptophan and their protecting group properties were investigated.Among them, 2,4,6-trimethoxybenzenesulfonyl and 4-methoxy-2,3,6-trimethylbenzenesulfonyl are stable to trifluoroacetic acid, but can be readily removed by hydrogen fluoride or methanesulfonic acid, and suppress decomposition and modification of the tryptophan residue during peptide synthesis.These protecting groups were successfully used in syntheses of bombesin, a potent analog of luteinizing hormone-releasing hormone by the solution method and dynorphin by the solid-phase method.Keywords-peptide synthesis; tryptophan; protecting group; 2,4,6-trimethoxybenzenesulfonyl group; 4-methoxy-2,3,6-trimethylbenzenesulfonyl group

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