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845754-77-0

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845754-77-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 845754-77-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,5,7,5 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 845754-77:
(8*8)+(7*4)+(6*5)+(5*7)+(4*5)+(3*4)+(2*7)+(1*7)=210
210 % 10 = 0
So 845754-77-0 is a valid CAS Registry Number.

845754-77-0Downstream Products

845754-77-0Relevant academic research and scientific papers

A new approach to 4-arylstyrenes: microwave-assisted synthesis and photophysical properties

Charushin, V. N.,Chistyakov, K. A.,Eddin, M. Zen,Pervova, M. G.,Rusinov, G. L.,Verbitskiy, E. V.,Zhilina, E. F.

, p. 2139 - 2144 (2022/01/22)

A convenient method was developed for the synthesis of 4-arylstyrenes containing residues of polycyclic aromatics or triphenylamine. The method is based on the microwave-assisted Suzuki—Miyaura cross-coupling reaction. The optical properties of the compou

Charge-transporting material and organic light-emitting device including the same

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Paragraph 0349-0351, (2017/03/25)

Disclosed are a charge transporting material and an organic light emitting device including the same. The organic light emitting device using the charge transporting material has a lower driving voltage and improved current efficiency and durability. The charge transporting material includes: a constituent unit (1) represented by below chemical formula 1 or 2; and a constituent unit (2) represented by below chemical formula 3 or 4.COPYRIGHT KIPO 2016

Polymers with alkyl main chain pendent biphenyl carbazole or triphenylamine unit as host for polymer light emitting diodes

Chuang, Ching-Nan,Chuang, Hsin-Jou,Chen, Szu-Hsien,Leung, Man-Kit,Hsieh, Kuo-Huang,Wang, Yu-Xun,Huang, Jau-Jiun

, p. 4983 - 4992,10 (2012/12/12)

The soluble styrene polymers, bearing dicarbazole, phenylcarbazole or phenyltriphenylamine side groups were investigated as a host material for green emitter in phosphorescent PLED devices. Those polymers were synthesized by free radical polymerization via azobisisobutyronitrile (AIBN) as initiator under 75 °C. All of the host materials exhibit high thermal stability with high decomposition (Td,5% weight loss > 398 °C) and glass transition temperatures (Tg > 172 °C). The HOMO (ca. -5.39 -5.69 eV) and LUMO (ca. -2.22 -2.41 eV) levels with the triplet energy of ca. 2.50-2.93 eV suggest that polymers are suitable for host materials for green emitter. The devices based on the emissive layers containing host materials doped with Ir(ppy)3 (4 wt%) display stable green emission with high device performances. The brightness and current efficiency reach 15,800 cd/m2 and 17.5 cd/A, respectively, at the optimum blending with 40 wt% 2-(4-biphenyl)-5-(4-tert-butylphenyl)-1,3,4-oxadiazol (t-PBD). Furthermore, the device performance reached higher brightness (23,400 cd/m2) and current efficiency (12.3 cd/A) when mixture with 2,4,6-triphenyl-1,3,5-triazine (TRZ) and t-PBD.

Living anionic polymerization of styrene derivatives containing triphenylamine moieties through introduction of protecting group

Kang, Beom-Goo,Kang, Nam-Goo,Lee, Jae-Suk

experimental part, p. 8400 - 8408 (2011/11/12)

We carried out the anionic polymerization of styrene derivatives containing the triphenylamine moieties, 4,4-vinylphenyltriphenylamine (A) and 4,4-vinylphenyl-N,N-bis(4-tert-butylphenyl)benzenamine (B), with a variety of initiators in tetrahydrofuran (THF

Arylamine compounds and their use in electronic devices

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Page/Page column 13-14, (2010/06/14)

Provided are arylamine compounds having Formula I, II, III, or IV: wherein Ar is the same or different at each occurrence and is aryl having from 6 to 30 carbon atoms or heteroaryl having from 2 to 30 carbon atoms. Also provided are compositions comprisin

CHARGE TRANSPORT MATERIALS

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Page/Page column 20-21, (2008/06/13)

Charge transport materials are provided, and methods for making the same.

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