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1,4-Phenylenebis(ethene-2,1-diyl)dianiline, also known as bisphenol A bis(2-hydroxyethyl)ether, is a chemical compound with the molecular formula C20H24N2O4. It is a colorless, viscous liquid that is soluble in water and organic solvents. 1,4-phenylenebis(ethene-2,1-diyl)dianiline is primarily used as a crosslinking agent in the production of epoxy resins, which are widely employed in various industries, including coatings, adhesives, and composite materials. It enhances the mechanical properties, thermal stability, and chemical resistance of the epoxy resins. Additionally, it is used as a curing agent for epoxy resins, promoting the formation of a three-dimensional network structure that imparts strength and durability to the final product.

67006-66-0

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67006-66-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67006-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,0 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67006-66:
(7*6)+(6*7)+(5*0)+(4*0)+(3*6)+(2*6)+(1*6)=120
120 % 10 = 0
So 67006-66-0 is a valid CAS Registry Number.

67006-66-0Downstream Products

67006-66-0Relevant academic research and scientific papers

Synthesis and characterization of a conjugated porphyrin dyad entangled with carboxyl functionalized benzimidazolium: An efficient metal free sensitizer for DSSCs

Bhuse, Darpan V.,Bhagat, Pundlik R.

, p. 1430 - 1445 (2021/02/06)

As an archetypal functional molecule, porphyrin is the nature's best photosynthetic pigment in plants, which mimics the principles of solar energy conversion. Considering the prodigious ability of porphyrin to harvest light, we present the stepwise synthesis of a novel conjugated meso-substituted porphyrin dyad entangled with carboxyl functionalized benzimidazolium moieties (CPDCFBM) as a sensitizer for application in a dye sensitised solar cell (DSSC). 1,4-Di(4-amidostyryl)benzene functionalised with a benzimidazole moiety served as a spacer between two substituted porphyrin moieties. The dyad was characterized using analytical techniques such as Fourier-transform infrared spectroscopy, ultraviolet-visible absorption spectroscopy, nuclear magnetic resonance spectroscopy, thermogravimetric analysis, BET surface area analysis, cyclic voltammetry (CV) studies and electrochemical impedance spectroscopy (EIS). The band gap measured using UV-vis spectroscopy was found to be 1.42 eV. The highest occupied molecular orbital and lowest unoccupied molecular orbital energy levels calculated from CV studies revealed that the frontier orbital energy levels make the system suitable for use as a sensitizer in conjugation with TiO2 in DSSCs. A DSSC fabricated using dyad sensitized TiO2 as an iodide tri-iodide redox couple exhibited a power conversion efficiency of 6.9%, under illumination (AM 1.5, 100 mW cm-2) with a sensitization time of 4 h without adding any efficiency booster and anti-aggregating agents. The strong tethering of the dyad to the TiO2 surface was achieved via linking through six carboxylate groups to form an envelope around TiO2 to ensure excellent electronic communication and good stability against the aggregation of the dyad. An EIS study demonstrated that the dyad shows faster electron injection than recombination. This journal is

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