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The chemical compound "2-<2-<2-(Benzyloxycarboxamido)-2-methylpropionamido>-2-methylpropionamido>-2-methylpropionsaeure" is a complex organic molecule with a long and intricate structure. It features a central 2-methylpropionic acid backbone, with two 2-methylpropionamido groups attached to it. One of these 2-methylpropionamido groups is further substituted with a benzyloxycarboxamido group. 2-<2-<2-(Benzyloxycarboxamido)-2-methylpropionamido>-2-methylpropionamido>-2-methylpropionsaeure is characterized by its multiple amide linkages and a benzyloxycarbonyl (Cbz) protecting group, which is commonly used in peptide synthesis to protect amino groups. The compound's structure suggests potential applications in pharmaceuticals or as a synthetic intermediate in the preparation of more complex molecules. Its exact properties and reactivity would depend on the specific context in which it is used, such as its role in a larger molecular assembly or its interaction with other chemical entities.

4512-41-8

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4512-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4512-41-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,1 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4512-41:
(6*4)+(5*5)+(4*1)+(3*2)+(2*4)+(1*1)=68
68 % 10 = 8
So 4512-41-8 is a valid CAS Registry Number.

4512-41-8Relevant academic research and scientific papers

Helical Peptides Design for Molecular Dipoles Functionalization of Wide Band Gap Oxides

Bartynski, Robert A.,Chen, Yuan,Galoppini, Elena,Harmer, Ryan,Rangan, Sylvie,Viereck, Jonathan

, p. 3489 - 3498 (2020/03/06)

The use of helical hexapeptides to establish a surface dipole layer on a TiO2 substrate, with the goal of influencing the energy levels of a coadsorbed chromophore, is explored. Two helical hexapeptides, synthesized from 2-amino isobutyric acid

Synthesis of poly-aib oligopeptides and aib-containing peptides via the 'azirine/oxazolone method', and their crystal structures

Dannecker-Doerig, Ingeborg,Linden, Anthony,Heimgartner, Heinz

experimental part, p. 993 - 1011 (2011/08/05)

The protected poly-Aib oligopeptides Z-(Aib)n-N(Me)Ph with n=2-6 were prepared according to the 'azirine/oxazolone method', i.e., by coupling amino or peptide acids with 2,2,N-trimethyl-N-phenyl-2H-azirin-3-amine (1a) as an Aib synthon (Schemea 2). Following the same concept, the segments Z-(Aib)3-OH (9) and H-L-Pro-(Aib)3-N(Me)Ph (20) were synthesized, and their subsequent coupling with N,N′- dicyclohexylcarbodiimide (DCC)/ZnCl2 led to the protected heptapeptide Z-(Aib)3-L-Pro-(Aib)3-N(Me)Ph (21; Schemea 3). The crystal structures of the poly-Aib oligopeptide amides were established by X-ray crystallography confirming the 310-helical conformation of Aib peptides.

3-(Dimethylamino)-2,2-dimethyl-2H-azirine as an Aib Equivalent; Synthesis of Aib Oligopeptides

Obrecht, Daniel,Heimgartner, Heinz

, p. 102 - 115 (2007/10/02)

3-(Dimethylamino)-2,2-dimethyl-2H-azirine (1) reacts with carboxylic acids at 0-25 degC to give 2-acylamino-N,N,2-trimethylpropionamides (=2-acylamino-N,N-dimethylisobutyramide, acyl-Aib-NMe2) in excellent yields (Scheme 2 and 3).Examples of α-amino-, α-h

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