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Triphenyl(3-chloro-4-aminophenyl)methane is a complex organic compound with the molecular formula C25H20ClN. It is characterized by a central carbon atom bonded to three phenyl groups and a 3-chloro-4-aminophenyl group. The 3-chloro-4-aminophenyl moiety features a chlorine atom at the third carbon and an amino group at the fourth carbon of the phenyl ring. triphenyl(3-chloro-4-aminophenyl)methane is significant in organic chemistry due to its potential applications in the synthesis of various pharmaceuticals and chemical intermediates. Its unique structure, with the combination of chlorine and amino groups, allows for further functionalization and reaction with other molecules, making it a valuable building block in the creation of more complex organic molecules.

95745-23-6

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95745-23-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95745-23-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,7,4 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 95745-23:
(7*9)+(6*5)+(5*7)+(4*4)+(3*5)+(2*2)+(1*3)=166
166 % 10 = 6
So 95745-23-6 is a valid CAS Registry Number.

95745-23-6Relevant academic research and scientific papers

Triphenyl moieties as building blocks for obtaining molecular glasses with nonlinear optical activity

Traskovskis, Kaspars,Mihailovs, Igors,Tokmakovs, Andrejs,Jurgis, Andrejs,Kokars, Valdis,Rutkis, Martins

, p. 11268 - 11276 (2012)

The incorporation of trityl and triphenylsilyl groups into low molecular weight molecules allows the formation of stable molecular glasses. A series of materials based on the N-phenyldiethanolamine core was synthesized bearing different azobenzenes and benzylydene-1,3-indandione as active chromophores. Molecular hyperpolarizability of the synthesized compounds was calculated by a restricted Hartree-Fock method with basis 6-31G(d,p) and measured in solutions by hyper-Rayleigh scattering. Non-linear optical (NLO) activity of the thin glassy films was confirmed after a corona poling procedure. Thermal sustainability of the NLO response of up to 85 °C was achieved. Quantum chemical calculations of the compounds revealed increased steric bulk and conformational freedom of the triphenylsilyl moiety. While the presence of the triphenylsilyl group results in more stable glasses and increased material nonlinearity, in the case of trityl groups, measured glass transition temperatures are higher.

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