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53558-76-2

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53558-76-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53558-76-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,5 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53558-76:
(7*5)+(6*3)+(5*5)+(4*5)+(3*8)+(2*7)+(1*6)=142
142 % 10 = 2
So 53558-76-2 is a valid CAS Registry Number.

53558-76-2Downstream Products

53558-76-2Relevant academic research and scientific papers

A Comprehensive Landscape for Fibril Association Behaviors Encoded Synergistically by Saccharides and Peptides

Liu, Rongying,Zhang, Ran,Li, Long,Kochovski, Zdravko,Yao, Lintong,Nieh, Mu-Ping,Lu, Yan,Shi, Tongfei,Chen, Guosong

supporting information, p. 6622 - 6633 (2021/05/29)

Nature provides us a panorama of fibrils with tremendous structural polymorphism from molecular building blocks to hierarchical association behaviors. Despite recent achievements in creating artificial systems with individual building blocks through self-

Building Nanowires from Micelles: Hierarchical Self-Assembly of Alternating Amphiphilic Glycopolypeptide Brushes with Pendants of High-Mannose Glycodendron and Oligophenylalanine

Liu, Yijiang,Zhang, Yufei,Wang, Zheyu,Wang, Jue,Wei, Kongchang,Chen, Guosong,Jiang, Ming

, p. 12387 - 12394 (2016/10/09)

Mimicking the diverse glyco-conjugate structures in nature is always the dream of scientists. Right now, hierarchical self-assembled structures of natural conjugates of peptides and sugars could not easily be achieved via linear glycopolypeptide with mono

Peptidehelicenes in solution and gel: chiral discrimination through interactions between two types of helixes

Nakagawa, Hiroko,Ohtsuka, Kumiko,Sugahara, Katsuhito,Kobayashi, Chika,Masuoka, Yuichi,Yamada, Koh-ichi,Kawase, Masami

experimental part, p. 659 - 664 (2010/08/06)

Helical [5]thiaheterohelicene 5HM, which rapidly interconverts between P and M enantiomers in solution, was connected to helical l-phenylalanine oligomers with an ester linkage to give peptidehelicenes (5Fn, where n: number of bonded phenylalanines). The

Stereoselective reduction of N-hydroxy-α-iminocarbonyl-oligopeptide methyl esters with Zn-MsOH

Kise, Naoki,Takaoka, Shuji,Yamauchi, Masahiro,Ueda, Nasuo

, p. 7297 - 7300 (2007/10/03)

The reduction of N-hydroxy-α-imino esters with Zn-MsOH in THF afforded α-amino esters in high yields. The reduction of N-hydroxy-α-iminocarbonyl-oligopeptide methyl esters prepared from L-phenylalanine and L-leucine di-, tri-, tetrapeptides gave the corre

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