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4-bromo-N,N-bis(4-(hexylthio)phenyl)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1354780-55-4

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1354780-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1354780-55-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,4,7,8 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1354780-55:
(9*1)+(8*3)+(7*5)+(6*4)+(5*7)+(4*8)+(3*0)+(2*5)+(1*5)=174
174 % 10 = 4
So 1354780-55-4 is a valid CAS Registry Number.

1354780-55-4Relevant academic research and scientific papers

Thiazolo[5,4-d]thiazole-based organic sensitizers with strong visible light absorption for transparent, efficient and stable dye-sensitized solar cells

Dessì, Alessio,Calamante, Massimo,Mordini, Alessandro,Peruzzini, Maurizio,Sinicropi, Adalgisa,Basosi, Riccardo,Fabrizi De Biani, Fabrizia,Taddei, Maurizio,Colonna, Daniele,Di Carlo, Aldo,Reginato, Gianna,Zani, Lorenzo

, p. 32657 - 32668 (2015)

A small set of thiazolo[5,4-d]thiazole-based D-π-A organic dyes, endowed with bis-pentylpropylenedioxythiophene (ProDOT) moieties in the π-spacer, was designed with the aid of computational analysis, synthesized and characterized. The presence of bulky an

Atomic level resolution of dye regeneration in the dye-sensitized solar cell

Robson, Kiyoshi C. D.,Hu, Ke,Meyer, Gerald J.,Berlinguette, Curtis P.

, p. 1961 - 1971 (2013/04/10)

Two donor-acceptor organic dyes have been synthesized that differ only by a two-heteroatom change from oxygen to sulfur within the donor unit. The two dyes, (E)-3-(5-(4-(bis(4-(hexyloxy)phenyl)amino)phenyl)thiophen-2-yl)-2- cyanoprop-2-enoic acid (Dye-O) and (E)-3-(5-(4-(bis(4-(hexylthio)phenyl)amino) phenyl)thiophen-2-yl)-2-cyanoprop-2-enoic acid) (Dye-S), were tested in solar cell devices employing both I3-/I--based and [Co(bpy)3]3+/2+ redox mediators. Power conversion efficiencies over 6% under simulated AM 1.5 illumination (1 Sun) were achieved in both electrolytes. Despite similar optical and redox properties for the two dyes, a consistently higher open-circuit voltage (Voc) was measured for Dye-S relative to Dye-O. The improved efficiency observed with Dye-S in an iodide redox mediator is against the commonly held view that sulfur atoms promote charge recombination attributed to inner-sphere interactions. Detailed mechanistic studies revealed that this is a consequence of a 25-fold enhancement of the regeneration rate constant that enhances the regeneration yield under open circuit conditions. The data show that a high short circuit photocurrent does not imply optimal regeneration efficiency as is often assumed.

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