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2-Benzyl-2-phenylcyclopentanone is a complex organic compound with the molecular formula C20H20O. It is a white crystalline solid that is derived from the cyclopentanone core, which is a five-membered ring with a ketone group. The molecule features a benzyl group (a phenylmethyl group) and a phenyl group attached to the same carbon atom of the cyclopentanone ring, which gives it a unique structure. 2-benzyl-2-phenylcyclopentanone is of interest in organic chemistry due to its potential applications in the synthesis of various pharmaceuticals and other organic compounds. It is typically synthesized through a series of chemical reactions, such as the aldol condensation of benzaldehyde with cyclopentanone, followed by further functional group transformations. The compound's properties, such as its melting point and solubility, can be influenced by the specific conditions under which it is synthesized and purified.

5359-14-8

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5359-14-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5359-14-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5359-14:
(6*5)+(5*3)+(4*5)+(3*9)+(2*1)+(1*4)=98
98 % 10 = 8
So 5359-14-8 is a valid CAS Registry Number.

5359-14-8Relevant academic research and scientific papers

Dual visible light photoredox and gold-catalyzed arylative ring expansion

Shu, Xing-Zhong,Zhang, Miao,He, Ying,Frei, Heinz,Toste, F. Dean

, p. 5844 - 5847 (2014/05/20)

A combination of visible light photocatalysis and gold catalysis is applied to a ring expansion-oxidative arylation reaction. The reaction provides an entry into functionalized cyclic ketones from the coupling reaction of alkenyl and allenyl cycloalkanols with aryl diazonium salts. A mechanism involving generation of an electrophilic gold(III)-aryl intermediate is proposed on the basis of mechanistic studies, including time-resolved FT-IR spectroscopy.

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