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878675-11-7

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878675-11-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 878675-11-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,8,6,7 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 878675-11:
(8*8)+(7*7)+(6*8)+(5*6)+(4*7)+(3*5)+(2*1)+(1*1)=237
237 % 10 = 7
So 878675-11-7 is a valid CAS Registry Number.

878675-11-7Relevant articles and documents

Dendron engineering in self-host blue iridium dendrimers towards low-voltage-driving and power-efficient nondoped electrophosphorescent devices

Wang, Yang,Wang, Shumeng,Ding, Junqiao,Wang, Lixiang,Jing, Xiabin,Wang, Fosong

, p. 180 - 183 (2016/12/27)

Dendron engineering in self-host blue Ir dendrimers is reported to develop power-efficient nondoped electrophosphorescent devices for the first time, which can be operated at low voltage close to the theoretical limit (Eg/e: corresponding to the optical bandgap divided by the electron charge). With increasing dendron's HOMO energy levels from B-POCz to B-CzCz and B-CzTA, effective hole injection is favored to promote exciton formation, resulting in a significant reduction of driving voltage and improvement of power efficiency. Consequently, the nondoped device of B-CzTA achieves extremely low driving voltages of 2.7/3.4/4.4 V and record high power efficiencies of 30.3/24.4/16.3 lm W?1 at 1, 100 and 1000 cd m?2, respectively. We believe that this work will pave the way to the design of novel power-efficient self-host blue phosphorescent dendrimers used for energy-saving displays and solid-state lightings.

3,6-Bis(indol-1-yl)-9-phenylcarbazoles as electroactive materials for electrophosphorescent diodes

Keruckas,Grazulevicius,Volyniuk,Cherpak,Stakhira

, p. 66 - 72 (2013/09/23)

Four derivatives of 3,6-bis(indol-1-yl)-9-phenylcarbazole were synthesized by Ullmann-type coupling including those having methoxy groups at the different positions. Thermal, optical and photophysical properties of the synthesized materials were studied.

N-phenyl triscarbazole

-

, (2012/04/10)

The present invention relates to a novel triscarbazole compound having substituent on N-phenyl, which can be represented by Formula (I). wherein R1 is selected from the group consisting of halogen or alkyl or alkoxy group having 1 to 20 carbon atoms wherein one or more hydrogen atom may be replaced by halogen; RA, RB, Rc, RD and RE are any of substituents; and i, j, k, l and m are same or different at each occurrence and represent an integer from 0 to 4. By introduction of the substituent on N-phenyl, the device efficiency, stability and lifetime can be increased while maintaining the solubility. These compounds can be used in various organic devices such as organic light emitting diodes, photovoltaic cells or organic semiconductor devices.

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