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Triphenyl-p-tolyl-methane, also known as triphenyl-4-methylbenzylmethane, is an organic compound characterized by a central carbon atom bonded to a p-tolyl (4-methylphenyl) group and three phenyl groups. This molecule is a derivative of triphenylmethane, with a methyl group attached to the para position of the phenyl ring. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. Triphenyl-p-tolyl-methane is synthesized through the reaction of p-tolylmagnesium bromide with triphenylchloromethane. It is used in the synthesis of various organic compounds and as a ligand in coordination chemistry. The compound is known for its stability and is often used in studies involving the properties of aryl groups and their interactions with other chemical entities.

82361-68-0

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82361-68-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82361-68-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,6 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82361-68:
(7*8)+(6*2)+(5*3)+(4*6)+(3*1)+(2*6)+(1*8)=130
130 % 10 = 0
So 82361-68-0 is a valid CAS Registry Number.

82361-68-0Relevant academic research and scientific papers

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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