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(+)-3-(diphenylphosphanyl)benzoyl-L-valine-n-butylamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1041871-67-3

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1041871-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1041871-67-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,1,8,7 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1041871-67:
(9*1)+(8*0)+(7*4)+(6*1)+(5*8)+(4*7)+(3*1)+(2*6)+(1*7)=133
133 % 10 = 3
So 1041871-67-3 is a valid CAS Registry Number.

1041871-67-3Downstream Products

1041871-67-3Relevant academic research and scientific papers

Supramolecular bidentate ligands by metal-directed in situ formation of antiparallel β-sheet structures and application in asymmetric catalysis

Laungani, Andy C.,Slattery, John M.,Krossing, Ingo,Breit, Bernhard

, p. 4488 - 4502 (2008)

The principles of protein structure design, molecular recognition, and supramolecular and combinatorial chemistry have been applied to develop a convergent metal-ion-assisted self-assembly approach that is a very simple and effective method for the de novo design and the construction of topologically predetermined antiparallel β-sheet structures and self-assembled catalysts. A new concept of in situ generation of bidentate P-ligands for transition-metal catalysis, in which two complementary, monodentate, peptide-based ligands are brought together by employing peptide secondary structure motif as constructing tool to direct the self-assembly process, is achieved through formation of stable β-sheet motifs and subsequent control of selectivity. The supramolecular structures were studied by 1H, 31P, and 13C NMR spectroscopy, ESI mass spectrometry, X-ray structure analysis, and theoretical calculations. Our initial catalysis results confirm the close relationship between the self-assembled sheet conformations and the catalytic activity of these metallopeptides in the asymmetric rhodium-catalyzed hydroformylation. Good catalyst activity and moderate enantioselectivity were observed for the selected combination of catalyst and substrate, but most importantly the concept of this new methodology was successfully proven. This work presents a perspective interface between protein design and supramolecular catalysis for the design of β-sheet mimetics and screening of libraries of self-organizing supramolecular catalysts.

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