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2,3-diphenyl-3a,4,7,7a-tetrahydro-1H-4,7-methanoinden-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41577-62-2

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41577-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41577-62-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,5,7 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41577-62:
(7*4)+(6*1)+(5*5)+(4*7)+(3*7)+(2*6)+(1*2)=122
122 % 10 = 2
So 41577-62-2 is a valid CAS Registry Number.

41577-62-2Relevant academic research and scientific papers

Synthesis, Coordination Study, and Catalytic Pauson-Khand Reactions of QuinoxP*(CO)4-μ-Alkyne Dicobalt Complexes

Gar?on, Martí,Cabré, Albert,Verdaguer, Xavier,Riera, Antoni

, p. 1056 - 1065 (2017/04/21)

The coordination of the P-stereogenic and sterically demanding bisphosphine QuinoxP* to μ-alkyne dicobalt hexacarbonyl complexes was studied experimentally and computationally. Whereas the coordination occurred exclusively in a chelating fashion, the diastereoselectivity was highly substrate dependent. However, it could be explained from the computed structure and energies of the different coordination modes. The fluxional behavior of these complexes was also studied computationally. Their performance as catalysts for the Pauson-Khand reaction was explored, and outstanding reactivity was observed. Although the asymmetric induction was low to moderate, the stereochemical outcome could be mechanistically rationalized. This report provides promising results in terms of reactivity and mechanistic understanding for further developments of highly active chiral catalysts for intermolecular Pauson-Khand reactions.

Heterobimetallic alkyne complexes inorganic synthesis: An asymmetric variant of the Pauson-Khand reaction

Rutherford, David T.,Christie, Steven D. R.

, p. 9805 - 9808 (2007/10/03)

The use of heterobimetallic alkyne complexes for the synthesis of cyclopentenones is described. The inherent chirality of the complexes has been used to effect high levels of stereocontrol in transformations giving optically enriched organic end products.

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