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1,3,5-tris[4-(5'-diphenylamino-2,2'-bithien-5-yl)phenyl]benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1002403-67-9

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1002403-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1002403-67-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,2,4,0 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1002403-67:
(9*1)+(8*0)+(7*0)+(6*2)+(5*4)+(4*0)+(3*3)+(2*6)+(1*7)=69
69 % 10 = 9
So 1002403-67-9 is a valid CAS Registry Number.

1002403-67-9Downstream Products

1002403-67-9Relevant academic research and scientific papers

New molecular materials for hole injection: The synthesis and in situ ESR-UV/Vis/NIR spectroelectrochemistry of 2-diarylaminothiophene-based starburst compounds

Rapta, Peter,Tabet, Ahacene,Hartmann, Horst,Dunsch, Lothar

, p. 4998 - 5007 (2007)

A series of 2-diarylaminothiophene-based starburst compounds 14-16 with a central triphenylamino-, benzene-, and 1,3,5-triphenylbenzene moiety, respectively, were prepared at moderate yields by a palladium-catalysed coupling reaction. Their electrochemical, optical and magnetic properties were studied with respect to their application as hole transport materials, using cyclic voltammetry and in situ ESR-UV/Vis/NIR spectroelectrochemistry. Although all prepared 2-diarylaminothiophene-based starburst compounds are structurally related, their electrochemical properties differ in their dependence on the central moiety. The number of reversible voltammetric peaks is diminished upon changing the central triphenylamino moiety of the starburst compounds to a central benzene or 1,3,5-triphenylbenzene moiety. The simultaneous multiple electron transfer as well as the location of the spins on the core moieties was detected in the oxidation of the 1,3,5-triphenylbenzene based starburst compound. The stability of the charged states increased substantially upon the incorporation of a thiophene moiety between the central moieties and the side groups. The Royal Society of Chemistry 2007.

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