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9-(4-methoxyphenyl)-9H-thioxanthene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52797-72-5

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52797-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52797-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,9 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52797-72:
(7*5)+(6*2)+(5*7)+(4*9)+(3*7)+(2*7)+(1*2)=155
155 % 10 = 5
So 52797-72-5 is a valid CAS Registry Number.

52797-72-5Downstream Products

52797-72-5Relevant academic research and scientific papers

Synthesis of new thioxanthenes by organocatalytic intramolecular Friedel–Crafts reaction

Yildiz, Tülay

, p. 2177 - 2188 (2018/07/21)

An efficient organocatalytic route has been developed to synthesize novel substituted thioxanthenes (2a–2v) starting from diaryl thioether alcohols (1a–1v) using the intramolecular Friedel–Crafts reaction. The starting materials were obtained in two stage

Graphene-Oxide-Catalyzed Direct CH?CH-Type Cross-Coupling: The Intrinsic Catalytic Activities of Zigzag Edges

Wu, Hongru,Su, Chenliang,Tandiana, Rika,Liu, Cuibo,Qiu, Chuntian,Bao, Yang,Wu, Ji'en,Xu, Yangsen,Lu, Jiong,Fan, Dianyuan,Loh, Kian Ping

supporting information, p. 10848 - 10853 (2018/08/17)

The development of graphene oxide (GO)-based materials for C?C cross-coupling represents a significant advance in carbocatalysis. Although GO has been used widely in various catalytic reactions, the scope of reactions reported is quite narrow, and the relationships between the type of functional groups present and the specific activity of the GO are not well understood. Herein, we explore CH?CH-type cross-coupling of xanthenes with arenes using GO as real carbocatalysts, and not as stoichiometric reactants. Mechanistic studies involving molecular analogues, as well as trapped intermediates, were carried out to probe the active sites, which were traced to quinone-type functionalities as well as the zigzag edges in GO materials. GO-catalyzed cross-dehydrogenative coupling is operationally simple, shows reusability over multiple cycles, can be conducted in air, and exhibits good functional group tolerance.

A classical but new kinetic equation for hydride transfer reactions

Zhu, Xiao-Qing,Deng, Fei-Huang,Yang, Jin-Dong,Li, Xiu-Tao,Chen, Qiang,Lei, Nan-Ping,Meng, Fan-Kun,Zhao, Xiao-Peng,Han, Su-Hui,Hao, Er-Jun,Mu, Yuan-Yuan

, p. 6071 - 6089 (2013/09/12)

A classical but new kinetic equation to estimate activation energies of various hydride transfer reactions was developed according to transition state theory using the Morse-type free energy curves of hydride donors to release a hydride anion and hydride acceptors to capture a hydride anion and by which the activation energies of 187 typical hydride self-exchange reactions and more than thirty thousand hydride cross transfer reactions in acetonitrile were safely estimated in this work. Since the development of the kinetic equation is only on the basis of the related chemical bond changes of the hydride transfer reactants, the kinetic equation should be also suitable for proton transfer reactions, hydrogen atom transfer reactions and all the other chemical reactions involved with breaking and formation of chemical bonds. One of the most important contributions of this work is to have achieved the perfect unity of the kinetic equation and thermodynamic equation for hydride transfer reactions. The Royal Society of Chemistry.

A new synthetic route to unsymmetrical 9-arylxanthenes

Das, Sajal Kumar,Singh, Ritesh,Panda, Gautam

scheme or table, p. 4757 - 4761 (2010/02/28)

A. facile and general three-step synthetic route towards unsymmetrical 9-arylxanthenes was developed. The reaction sequence involves nucleophilic substitution of commercially available 2-fluorobenzaldehydes with arenoxides, Grignard reaction of the resulting 2-arenoxybenzaldehydes with arylmagnesium bromides, followed by FeCl3-catalyzed intramolecular diarylmethylation of the resulting carbinols, This strategy was extended to access symmetrical as well as unsymmetrical 9-arylthioxanthenes.

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