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4,4'-(quinoxaline-5,8-diyl)bis(N,N-diphenylaniline) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1236771-88-2

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1236771-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1236771-88-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,6,7,7 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1236771-88:
(9*1)+(8*2)+(7*3)+(6*6)+(5*7)+(4*7)+(3*1)+(2*8)+(1*8)=172
172 % 10 = 2
So 1236771-88-2 is a valid CAS Registry Number.

1236771-88-2Downstream Products

1236771-88-2Relevant academic research and scientific papers

Red-light-emitting system based on aggregation of donor-acceptor derivatives in polar aqueous media

Ishi-I, Tsutomu,Ikeda, Kei,Kichise, Yuki,Ogawa, Michiaki

, p. 1553 - 1557 (2012)

Glowing together: An efficient red-light-emitting system has been created in polar water media based on the aggregation of donor-acceptor molecules. In the THF/water mixture, the emission was quenched when a small volume of water was used, whereas it was

Controlling the charge transfer in D-A-D chromophores based on pyrazine derivatives

Lu, Xuefeng,Fan, Suhua,Wu, Jinhong,Jia, Xiaowei,Wang, Zhong-Sheng,Zhou, Gang

, p. 6480 - 6489 (2014)

A series of symmetrical donor-acceptor-donor (D-A-D) chromophores bearing various electron-withdrawing groups, such as quinoxaline (Qx), benzo[g]quinoxaline (BQ), phenazine (Pz), benzo[b]phenazine (BP), thieno[3,4-b]pyrazine (TP), and thieno[3,4-b]quinoxaline (TQ), has been designed and synthesized. Intramolecular charge transfer (ICT) interactions can be found for all the chromophores due to the electron-withdrawing properties of the two imine nitrogens in the pyrazine ring and the electron-donating properties of the other two amine nitrogens in the two triphenylamines. Upon the fusion of either benzene or thiophene ring on the pyrazine acceptor unit, the ICT interactions are strengthened, which results in the bathochromically shifted ICT band. Moreover, the thiophene ring is superior to the benzene ring in enlarging the ICT interaction and expanding the absorption spectrum. Typically, when a thiophene ring is fused on the Qx unit in DQxD, a near-infrared dye is realized in simple chromophore DTQD, which displays the maximum absorption wavelength at 716 nm with the threshold over 900 nm. This is probably due to the enhanced charge density on the acceptor moiety and better orbital overlap, as revealed by theoretical calculation. These results suggest that extending the conjugation of a pyrazine acceptor in an orthogonal direction to the D-A-D backbone can dramatically improve the ICT interactions.

Light-emitting properties of donor-acceptor and donor-acceptor-donor dyes in solution, solid, and aggregated states: Structure-property relationship of emission behavior

Ishi-I, Tsutomu,Ikeda, Kei,Ogawa, Michiaki,Kusakaki, Yutarou

, p. 89171 - 89187 (2015/11/09)

In this paper, we report a systematic study on the light-emitting behavior of a series of triphenylamine-based donor-acceptor-type dyes in the solution and solid states as well as in the aggregated state in polar aqueous media. The emission band shifted b

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