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N2,N4-dibutyl-N6,N6-diphenyl-1,3,5-triazine-2,4,6-triamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1361016-92-3

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1361016-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1361016-92-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,1,0,1 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1361016-92:
(9*1)+(8*3)+(7*6)+(6*1)+(5*0)+(4*1)+(3*6)+(2*9)+(1*2)=123
123 % 10 = 3
So 1361016-92-3 is a valid CAS Registry Number.

1361016-92-3Relevant academic research and scientific papers

Enhancement of photovoltaic properties in supramolecular polymer networks featuring a solar cell main-chain polymer H-bonded with conjugated cross-linkers

Patra, Dhananjaya,Ramesh, Mohan,Sahu, Duryodhan,Padhy, Harihara,Chu, Chih-Wei,Wei, Kung-Hwa,Lin, Hong-Cheu

, p. 1219 - 1228 (2012)

Stille polymerization was employed to synthesize a low-band-gap (LBG) conjugated main-chain polymer PBTH consisting of bithiazole, dithieno[3,2-b:2′,3′-d]pyrroles (DTP), and pendent melamine derivatives. Novel supramolecular polymer networks PBTH/C and PBTH/F were developed by mixing proper molar amounts of polymer PBTH (containing melamine pendants) to be hydrogen-bonded (H-bonded) with complementary uracil-based conjugated cross-linkers C and F (i.e., containing two symmetrical uracil moieties connected with carbazole and fluorene units through triple bonds). The formation of multiple H-bonds between polymer PBTH and cross-linkers C or F was confirmed by FT-IR measurements. In contrast to polymer PBTH, the supramolecular design with multiple H-bonds can enhance the photovoltaic properties of polymer solar cell (PSC) devices containing H-bonded polymer networks PBTH/C and PBTH/F by tuning their light harvesting capabilities, HOMO energy levels, and crystallinities. Initially, the power conversion efficiency (PCE) values of PSC devices containing supramolecular polymer networks PBTH/C and PBTH/F as electron donors and [6,6]-phenyl-C71-butyric acid methyl ester (PC 70BM) as an electron acceptor (polymer:PC70BM = 1:1 w/w) are found to be 0.97 and 0.68%, respectively, in contrast to 0.52% for polymer PBTH. The highest PCE value of 1.56% with a short-circuit current densities (Jsc) value of 7.16 mA/cm2, a open circuit voltages (Voc) value of 0.60 V, and a fill factor (FF) of 0.36 was further optimized in the PSC device containing a supramolecular polymer network PBTH/C as polymer:PC70BM = 1:2 w/w. These results indicate that supramolecular design is an effective route towards better photovoltaic properties of Voc, Jsc, and PCE values in polymer solar cells.

Synthesis and applications of a novel supramolecular polymer network with multiple H-bonded melamine pendants and uracil crosslinkers

Patra, Dhananjaya,Ramesh, Mohan,Sahu, Duryodhan,Padhy, Harihara,Chu, Chih-Wei,Wei, Kung-Hwa,Lin, Hong-Cheu

, p. 967 - 975 (2012/05/31)

A conjugated main-chain copolymer (PBT) consisting of bithiazole, dithieno[3,2-b:2′,3′-d]pyrroles (DTP), and pendent melamine units was synthesized by Stille polymerization, which can be hydrogen-bonded (H-bonded) with proper molar amounts of bi-functiona

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