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(S)-perfluorophenyl 2-((S)-2-((tert-butoxycarbonyl)amino)propanamido)propanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1620161-80-9

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1620161-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1620161-80-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,0,1,6 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1620161-80:
(9*1)+(8*6)+(7*2)+(6*0)+(5*1)+(4*6)+(3*1)+(2*8)+(1*0)=119
119 % 10 = 9
So 1620161-80-9 is a valid CAS Registry Number.

1620161-80-9Relevant academic research and scientific papers

Phosphonopeptides revisited, in an era of increasing antimicrobial resistance

Anderson, Rosaleen J.,Bedernjak, Alexandre F.,Cummings, Stephen P.,Day, Kathryn M.,Gray, Mark,Jones, Amanda L.,Marrs, Emma C. L.,Perry, John D.,Varadi, Linda

, (2020)

Given the increase in resistance to antibacterial agents, there is an urgent need for the development of new agents with novel modes of action. As an interim solution, it is also prudent to reinvestigate old or abandoned antibacterial compounds to assess

The effect of monosaccharides on self-assembly of benzenetricarboxamides

Wang, Jue,Qi, Wenjing,Chen, Guosong

supporting information, p. 587 - 591 (2019/01/04)

The interaction between monosaccharides exhibits an important role in the assembly of monosaccharide-containing molecules. In this work, three common monosaccharides, glucose, galactose and mannose, are employed to investigate the effect of monosaccharide on the self-assembly of benzenetricarboxamide (BTA) core-containing molecules. In the presence of monosaccharides, three benzenetricarboxamide derivatives aggregate into different ordered structures. When alanine linkers are introduced to these molecules between the core and the monosacchride, morphologies of three types of monosaccharide BTAs turned to disordered, meanwhile their structures become similar with the increase of the length of alanine linkers, indicating the disappearance of the monosaccharide effects.

Facile and mild synthesis of linear and cyclic peptides via thioesters

Agrigento, Paola,Albericio, Fernando,Chamoin, Sylvie,Dacquignies, Isabelle,Koc, Halil,Eberle, Martin

supporting information, p. 3922 - 3925 (2014/08/18)

Thioester-mediated peptide bond formation has recently garnered a lot of attention, most notably in its relevance to condensation of large peptide fragments. Herein, a simple and general ligation method for the preparation of linear and cyclic peptides, starting from peptide thioester, mainly p-chlorophenyl, precursors is reported. The inherent advantages of this method are the low epimerization, reduced dimerization, use of mild reaction conditions, and elimination of superfluous coupling reagents.

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