1361418-07-6 Usage
General Description
7-Bromo-4,4,9,9-tetrakis(4-hexylphenyl)-4,9-dihydro-s-indaceno[1,2-b:5,6-b']dithiophene-2-carbaldehyde is a chemical compound with a complex molecular structure. It contains a bromine atom and four hexylphenyl groups attached to a s-indaceno dithiophene backbone. Additionally, it has a carbaldehyde functional group at the 2-position. 7-Bromo-4,4,9,9-tetrakis(4-hexylphenyl)-4,9-dihydro-s-indaceno[1,2-b:5,6-b']dithiophene-2-carbaldehyde is likely to have applications in the field of organic semiconductors and organic electronics due to its conjugated structure and potential for use in organic photovoltaic devices and field-effect transistors. However, it may also have specific uses in the academic or industrial research settings for the synthesis of new materials with tailored electronic properties. The exact properties and potential applications of this compound may vary depending on its specific characteristics and the conditions under which it is used.
Check Digit Verification of cas no
The CAS Registry Mumber 1361418-07-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,1,4,1 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1361418-07:
(9*1)+(8*3)+(7*6)+(6*1)+(5*4)+(4*1)+(3*8)+(2*0)+(1*7)=136
136 % 10 = 6
So 1361418-07-6 is a valid CAS Registry Number.
1361418-07-6Relevant articles and documents
Tunable light-harvesting polymers containing embedded dipolar chromophores for polymer solar cell applications
Zeigler, David F.,Chen, Kung-Shih,Yip, Hin-Lap,Zhang, Yong,Jen, Alex K.-Y.
experimental part, p. 1362 - 1373 (2012/06/16)
A series of light-harvesting conjugated polymers were designed and synthesized for polymer solar cells. These newly designed polymers comprise an unusual two-dimensional conjugated structure with an electron-rich thiophene-triphenylamine backbone and stable planar indacenodithiophene π-bridges terminated with tunable electron acceptors. It was found that the electron-withdrawing strength of the acceptor could be used to manipulate the energy level of the lowest unoccupied molecular orbital and bandgap (as much as 0.3 eV), generating derivatives with complementary absorbance in the visible spectrum. This approach provides great flexibility in fine tuning the electronic and optical properties of the resultant polymers and facilitates the investigation of how these chemical modifications alter the subsequent photovoltaic properties of these materials.
