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[2-(propan-2-yl)phenyl]lithium is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41285-22-7

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41285-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41285-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,2,8 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41285-22:
(7*4)+(6*1)+(5*2)+(4*8)+(3*5)+(2*2)+(1*2)=97
97 % 10 = 7
So 41285-22-7 is a valid CAS Registry Number.

41285-22-7Downstream Products

41285-22-7Relevant academic research and scientific papers

Pyridylamino IVB group binuclear metal complex and preparation and application thereof

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Paragraph 0117; 0125-0127, (2020/11/12)

The invention relates to a pyridylamino IVB group binuclear metal complex and the preparation and the application thereof. The structure of the pyridylamino IVB group binuclear metal complex is shownas a formula I, and the pyridylamino IVB group binuclear

Stereostructure and thermodynamic stability of atropisomers of ortho-substituted 2,2′-diaryl-1,1′-binaphthalenes

Ehn, Marcel,Vassilev, Nikolay Georgiev,Kasak, Peter,Horvath, Branislav,Filo, Juraj,Mereiter, Kurt,Rakovsky, Erik,Putala, Martin

, p. 1303 - 1311 (2013/11/19)

A series of ortho-substituted 2,2′-aryl-1,1′-binaphthalenes were prepared via Negishi arylation of 2,2′-diiodo-1,1′- binaphthalene in good to high yields (65-95%) as an equilibrium mixtures of up to three atropisomers (unlike,unlike, like,unlike, and like,like). Thermodynamic stability parameters of the atropisomers were evaluated from VT NMR spectra by regression analysis. The DFT parameters calculated using CAM-B3LYP functional comprising solvent permittivity were, apart from the toluene solution, which was expected to interact with the aromatic solute, in qualitative agreement with the experimental values. In the case of the ditolyl derivative, the population of the atropisomers was confirmed by CD spectroscopy via comparison with the population-weighted averaged spectrum computed using the M06 functional. X-ray structure analyses of particular atropisomers of the dianisyl, dianilinyl, and dinaphthyl derivatives are also presented and discussed.

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