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The chemical "2-(4-Dicyanomethylene-cyclohexa-2,5-dienylidene)-malononitrile; compound with [2,2']bipyridinyl" is a complex organic compound consisting of a malononitrile moiety with a dicyanomethylene-cyclohexa-2,5-dienylidene group attached to its 2-position. 2-(4-Dicyanomethylene-cyclohexa-2,5-dienylidene)-malononitrile; compound with [2,2']bipyridinyl forms a complex with [2,2']bipyridinyl, a bidentate ligand that can chelate metal ions. The combination of these two components results in a molecule with potential applications in coordination chemistry, as it can form stable complexes with various metal ions. The structure of 2-(4-Dicyanomethylene-cyclohexa-2,5-dienylidene)-malononitrile; compound with [2,2']bipyridinyl is characterized by its conjugated system and the presence of multiple cyano groups, which contribute to its electronic properties and reactivity.

1930-34-3

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1930-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1930-34-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,3 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1930-34:
(6*1)+(5*9)+(4*3)+(3*0)+(2*3)+(1*4)=73
73 % 10 = 3
So 1930-34-3 is a valid CAS Registry Number.

1930-34-3Downstream Products

1930-34-3Relevant academic research and scientific papers

Electrochemical Behavior of Donor-Tetracyanoquinodimethane Electrodes in Aqueous Media

Jaeger, Calvin D.,Bard, Allen J.

, p. 5435 - 5442 (2007/10/02)

Electrodes prepared as compacted pellets from conductive donor-acceptor complexes of tetraquinodimethane (TCNQ) with several donors (D) (tetrathiotetracene, acridine, quinoline, N-methylphenazine, 2,2'- and 4,4'-bipyridine) were investigated in aqueous solutions.The results were compared to those of a previous investigation of TTF-TCNQ pellets (TTF = tetrathiafulvalene) and to results on single crystals of TTF-TCNQ reported here.The electrodes are stable over a potential region in which they could be employed as inert electrodes.The potential limits depended upon the stabilization gained upon complexation and the relative electrode potentials of the constituent compounds.Upon exceeding the potential limits of stability of the electrode, the electrode was reduced or oxidized.Subsequent voltammograms showed peaks attributable to insoluble compounds formed on the electrode surface.The potentials observed for the redox processes could be correlated to the degree of charge transfer, ρ, as well as gas-transfer ionization potentials and electron affinities.

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