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2-Thiophenecarboxaldehyde, 4-octyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

182483-20-1

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182483-20-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 182483-20-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,4,8 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 182483-20:
(8*1)+(7*8)+(6*2)+(5*4)+(4*8)+(3*3)+(2*2)+(1*0)=141
141 % 10 = 1
So 182483-20-1 is a valid CAS Registry Number.

182483-20-1Downstream Products

182483-20-1Relevant academic research and scientific papers

Efficient organic photovoltaic cells based on thiazolothiazole and benzodithiophene copolymers with π-conjugated bridges

Park, Junhoo,Park, Jong Baek,Ha, Jong-Woon,Park, Hea Jung,Kang, In-Nam,Hwang, Do-Hoon

, p. 1978 - 1988 (2018)

New donor–π–acceptor (D–π–A) type conjugated copolymers, poly[(4,8-bis((2-hexyldecyl)oxy)benzo[1,2-b:4,5-b′]dithiophene)-alt-(2,5-bis(4-octylthiophen-2-yl)thiazolo[5,4-d]thiazole)] (PBDT-tTz), and poly[(4,8-bis((2-hexyldecyl)oxy)benzo[1,2-b:4,5-b′]dithiophene)-alt-(2,5-bis(6-octylthieno[3,2-b]thiophen-2-yl)thiazolo[5,4-d]thiazole)] (PBDT-ttTz) were synthesized and characterized with the aim of investigating their potential applicability to organic photovoltaic active materials. While copolymer PBDT-tTz showed a zigzagged non-linear structure by thiophene π-bridges, PBDT-ttTz had a linear molecular structure with thieno[3,2-b]thiophene π-bridges. The optical, electrochemical, morphological, and photovoltaic properties of PBDT-tTz and PBDT-ttTz were systematically investigated. Furthermore, bulk heterojunction photovoltaic devices were fabricated by using the synthesized polymers as p-type donors and [6,6]-phenyl-C71-butyric acid methyl ester as an n-type acceptor. PBDT-ttTz showed a high power conversion efficiency (PCE) of 5.21% as a result of the extended conjugation arising from the thienothiophene π-bridges and enhanced molecular ordering in the film state, while PBDT-tTz showed a relatively lower PCE of 2.92% under AM 1.5 G illumination (100 mW/cm2).

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