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Triphenyl-(4-trifluoromethyl-phenyl)-methane is a complex organic compound characterized by its molecular formula C29H21F3. triphenyl-(4-trifluoromethyl-phenyl)-methane features a central methane molecule with three phenyl groups attached to it, one of which is substituted with a trifluoromethyl group at the para position. The presence of the trifluoromethyl group imparts unique electronic and steric properties to the molecule, which can significantly influence its chemical reactivity and physical behavior. The compound is of interest in various fields, including organic synthesis, materials science, and potentially as a precursor in the development of pharmaceuticals or specialty chemicals. Its structure provides a platform for further functionalization and exploration of its properties in different chemical environments.

2924-32-5

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2924-32-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2924-32-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,2 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2924-32:
(6*2)+(5*9)+(4*2)+(3*4)+(2*3)+(1*2)=85
85 % 10 = 5
So 2924-32-5 is a valid CAS Registry Number.

2924-32-5Downstream Products

2924-32-5Relevant 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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