1190978-93-8 Usage
General Description
5,6-bis(hexyloxy)benzo[c][1,2,5]thiadiazole is a chemical compound with the molecular formula C18H26N2O2S. It belongs to the class of benzo[c][1,2,5]thiadiazole, which are widely used as components in organic electronic devices, such as organic photovoltaic cells and organic field-effect transistors. This specific compound has two hexyloxy (C6H13O) groups attached to the benzene ring, and a thiadiazole moiety in the core structure. The hexyloxy substituents provide solubility and good film-forming properties, while the thiadiazole core contributes to its electron-accepting capabilities. These properties make 5,6-bis(hexyloxy)benzo[c][1,2,5]thiadiazole a promising candidate for use in organic electronic devices for its potential to enhance device performance.
Check Digit Verification of cas no
The CAS Registry Mumber 1190978-93-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,9,7 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1190978-93:
(9*1)+(8*1)+(7*9)+(6*0)+(5*9)+(4*7)+(3*8)+(2*9)+(1*3)=198
198 % 10 = 8
So 1190978-93-8 is a valid CAS Registry Number.
1190978-93-8Relevant articles and documents
High-performance dye-sensitized solar cells based on 5,6-bis-hexyloxy- benzo[2,1,3]thiadiazole
Chou, Hsien-Hsin,Chen, Yung-Chung,Huang, Hsuan-Jui,Lee, Ting-Hui,Lin, Jiann T.,Tsai, Chiitang,Chen, Kellen
supporting information; experimental part, p. 10929 - 10938 (2012/08/07)
New dipolar compounds containing a 5,6-bis-hexyloxy-benzo[2,1,3]thiadiazole entity in the conjugated spacer between the electron donating arylamine and the electron accepting 2-cyanoacrylic acid have been synthesized. These compounds were used as the sensitizers for efficient dye-sensitized solar cells. Compared to the congeners without the hexyloxy chains, the new dyes effectively suppress the dark currents and significantly improve the cell performance. The best conversion efficiency reached ~92% of the N719-based standard DSSC fabricated and measured under similar conditions (AM 1.5 irradiation). The Royal Society of Chemistry 2012.