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1,5-Bis-diphenylphosphonio-anthracen is a complex organic compound with the chemical formula C38H28P2. It is a derivative of anthracene, a tricyclic aromatic hydrocarbon, with two diphenylphosphonio groups attached at the 1 and 5 positions. 1,5-Bis-diphenylphosphonio-anthracen is characterized by its unique structure, which features a central anthracene core with two phosphonium groups attached to it through phenyl rings. The presence of phosphonium groups imparts interesting properties to the molecule, such as potential applications in organophosphorus chemistry and as a building block for more complex structures. The compound is typically synthesized through various chemical reactions and can be used in the development of new materials or as a precursor in the synthesis of other phosphorus-containing compounds.

1183-21-7

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1183-21-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1183-21-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,8 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1183-21:
(6*1)+(5*1)+(4*8)+(3*3)+(2*2)+(1*1)=57
57 % 10 = 7
So 1183-21-7 is a valid CAS Registry Number.

1183-21-7Downstream Products

1183-21-7Relevant academic research and scientific papers

Multi-Stage Redox Systems Based on Dicationic P-Containing Polycyclic Aromatic Hydrocarbons

Bouit, Pierre-Antoine,Caytan, Elsa,Delouche, Thomas,Hissler, Muriel,Jacquemin, Denis,Le Guennic, Boris,Roisnel, Thierry,Vacher, Antoine

supporting information, (2020/06/25)

We report the straightforward synthesis of unprecedented electron-acceptors based on dicationic P-containing PAHs (Polycyclic Aromatic Hydrocarbons) based on copper mediated radical approach. In these systems, two phosphoniums are connected through various PAHs backbones. The impact of π-extension on both the optical and redox properties is investigated using a joint experimental (UV/Vis absorption, fluorescence and cyclic voltammetry) and theoretical approach (TD-DFT calculations). Finally, (spectro)-electrochemical studies prove that these compounds possess three redox states and EPR studies confirm the in situ formation of an organic radical delocalized on the PAH backbone.

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