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(3-methylphenyl)triphenylmethane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

115228-92-7

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115228-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115228-92-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,2,2 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 115228-92:
(8*1)+(7*1)+(6*5)+(5*2)+(4*2)+(3*8)+(2*9)+(1*2)=107
107 % 10 = 7
So 115228-92-7 is a valid CAS Registry Number.

115228-92-7Relevant academic research and scientific papers

Understanding the desulphurization process in an ionic porous aromatic framework

Tian, Yuyang,Song, Jian,Zhu, Youliang,Zhao, Huanyu,Muhammad, Faheem,Ma, Tingting,Chen, Mo,Zhu, Guangshan

, p. 606 - 613 (2019)

An ionic porous aromatic framework, iPAF-1, was successfully synthesized from a designed monomer with imidazolium functional groups. The iPAF-1 exhibits the highest dibenzothiophene uptake among all reported adsorptive desulphurization adsorbents. The so-

The fabrication of IMo6?iPAF-1 as an enzyme mimic in heterogeneous catalysis for oxidative desulfurization under O2or air

Bawa, Mbage,Jiang, Mengting,Li, Yue,Song, Jian,Tian, Yuyang,Wang, Xiaohong,Zhu, Guangshan

, p. 9813 - 9824 (2020/06/05)

Na5[IMo6O24]·3H2O and a porous aromatic framework (iPAF-1) were used to build an off-the-shelf building material (IMo6?iPAF-1) to realize the highly efficient oxidation of organic sulfurs like oxygena

Synthesis of tetraarylmethanes via a Friedel-Crafts cyclization/desulfurization strategy

Griffin, Paul J.,Fava, Matthew A.,Whittaker, St. John T.,Kolonko, Kristopher J.,Catino, Arthur J.

, p. 3999 - 4002 (2018/10/02)

Tetraarylmethanes are an important class of molecules that contain four aryl groups bonded to a central carbon atom. The shape/three-dimensionality of these molecules makes them suitable for organic light-emitting diodes (OLEDs), organic solar cells, hydrogen storage, and even drug-delivery. Despite their importance, there are only a few methods available for their preparation. Herein, we report a simple procedure for the preparation of tetraarylmethanes that involves a bismuth-catalyzed Friedel-Crafts cyclization followed by a desulfurization reaction mediated by Raney nickel.

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