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4-{[4-(diphenylamino)phenyl](phenyl)amino}benzyl hex-5-ynoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1376711-36-2

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1376711-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1376711-36-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,6,7,1 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1376711-36:
(9*1)+(8*3)+(7*7)+(6*6)+(5*7)+(4*1)+(3*1)+(2*3)+(1*6)=172
172 % 10 = 2
So 1376711-36-2 is a valid CAS Registry Number.

1376711-36-2Downstream Products

1376711-36-2Relevant academic research and scientific papers

Click synthesis and reversible electrochromic behaviors of novel polystyrenes bearing aromatic amine units

Li, Yongrong,Michinobu, Tsuyoshi

, p. 2111 - 2120 (2012)

Novel electrochromic polymers were prepared by the click postfunctionalization of poly(4-azidomethylstyrene) with alkyne-containing aromatic amine units in the presence of Cu(I) catalysts. Two kinds of aromatic amine units, tris(4-alkoxyphenyl)amine and N,N,N',N'-tetraphenyl-p- phenylenediamine, were introduced into polystyrene side chains, which were completely characterized by gel permeation chromatography-multiangle light scattering, nuclear magnetic resonance, and infrared spectroscopies, and elemental analysis. Thermal analyses demonstrated the high stability with the decomposition temperatures exceeding 300 °C even after postfunctionalization. The UV-vis absorption spectra of the polymer thin films revealed negligible absorption in the visible region, as reasonably confirmed by visual observation. The polymer thin films were prepared by spray-coating on an indium tin oxide-coated glass plate. Cyclic voltammograms of these films exhibited anodic peaks ascribed to the oxidation of the side-chain aromatic amine moieties. The tris(4-alkoxyphenyl)amine unit displayed one-step oxidation at 0.287 V (vs. Ag/AgCl), while the N,N,N',N'-tetraphenyl-p-phenylenediamine unit showed two-step oxidations at 0.297 and 0.641 V. These oxidation processes produced new colors of the polymer films. The former triarylamine-based chromophore provided a blue color after the oxidation, while the latter phenylenediamine-based chromophore showed a potentially controlled green and dark blue colors. The reversibility and switching behaviors of these color changes were also comprehensively investigated. 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 Aromatic amine-based active electrochromophores were quantitatively introduced into a polystyrene side chain by using the Cu(I)-catalyzed azide-alkyne cycloaddition reaction. The reversible electrochromic behaviors of the functionalized polystyrenes were investigated by spectroelectrochemistry. Copyright

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