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2-cyclopentyl-1,1-diphenylethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59137-57-4

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59137-57-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59137-57-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,3 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59137-57:
(7*5)+(6*9)+(5*1)+(4*3)+(3*7)+(2*5)+(1*7)=144
144 % 10 = 4
So 59137-57-4 is a valid CAS Registry Number.

59137-57-4Relevant academic research and scientific papers

Homogeneous Rate Constants for Coupling between Electrochemically Generated Aromatic Anion Radicals and Alkyl Radicals

Pedersen, Steen U.,Lund, Torben

, p. 397 - 402 (2007/10/02)

Rate constants have been measured for the coupling between hexenyl radicals and 2,2-dimethylhexenyl radicals and electrogenerated anion radicals of anthracene, 9,10-diphenylanthracene, benzophenone and quinoxaline.The rate constant for all four reactions in N,N-dimethylformamide is log k2 = 9.1(5), which is in accordance previous results in 1,2-dimethoxyethane for naphthalene and benzophenone anion radicals and 1-hexenyl radicals.The data indicate that the redox potential of the aromatic anion radical has only a minor influence on the rate of coupling with alkyl radicals.The rate constants for anion radicals of 9,10-diphenylanthracene and benzophenone were somewhat lower, 6(1) x 108 M-1 s-1, which for 9,10-diphenylanthracene might be caused by steric hindrance by the two phenyl groups.The conclusion is that the coupling reaction between aromatic anion radicals and alkyl radicals has all the characteristics of a radical-radical coupling.

RADIKALISCHE REAKTIONSWEGE BEI THERMISCH INDUZIERTEN UMSETZUNGEN VON ZIRCONOCENKOMPLEXEN

Erker, G.,Rosenfeldt, F.

, p. 1285 - 1292 (2007/10/02)

The formation of products 2, 3 and 4(a-l) from both the reaction of εta2-bezophenone zirconocene 1 with alkyl halides and the thermolysis of the α-(Cp2ZrCl)-substituted benzhydrylmethylether 9, the latter proceeding with anchimeric assistance of the metal, can be understood assuming a stepwise reaction path through radical intermediates.The proposed intermediate transition-metal benzophenone ketyl 12 exhibits a reaction pattern differing from analogous main-group-metal ketyls.

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