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9H-Carbazole-9-carboxylic acid, 3,6-dibromo-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

161992-35-4

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161992-35-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161992-35-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,9,9 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 161992-35:
(8*1)+(7*6)+(6*1)+(5*9)+(4*9)+(3*2)+(2*3)+(1*5)=154
154 % 10 = 4
So 161992-35-4 is a valid CAS Registry Number.

161992-35-4Relevant academic research and scientific papers

Functionalization of biphenylcarbazole (CBP) with siloxane-hybrid chains for solvent-free liquid materials

Correia, Gabriel,Heinrich, Beno?t,Méry, Stéphane,Mager, Lo?c,Polychronopoulou, Kyriaki,Ribierre, Jean-Charles,Shaya, Janah

, (2021/12/29)

We report herein the synthesis of siloxane-functionalized CBP molecules (4,4′-bis(carbazole)-1,1′-biphenyl) for liquid optoelectronic applications. The room-temperature liquid state is obtained through a convenient functionalization of the molecules with heptamethyltrisiloxane chains via hydrosilylation of alkenyl spacers. The synthesis comprises screening of metal-catalyzed methodologies to introduce alkenyl linkers into carbazoles (Stille and Suzuki Miyaura cross-couplings), incorporate the alkenylcarbazoles to dihalobiphenyls (Ullmann coupling), and finally introduce the siloxane chains. The used conditions allowed the synthesis of the target compounds, despite the high reactivity of the alkenyl moieties bound to π-conjugated systems toward undesired side reactions such as polymerization, isomerization, and hydrogenation. The features of these solvent-free liquid CBP derivatives make them potentially interesting for fluidic optoelectronic applications.

ORGANIC COMPOUND, LIGHT EMITTING DIODE AND LIGHT EMITTING DEVICE HAVING THE COMPOUND

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Paragraph 0197-0198, (2020/07/07)

The present disclosure relates to an organic compound having a binaphthyl core and a group connected to the biphenyl core and having excellent charge mobility property, and a light emitting diode and a light emitting device having the organic compound. The organic compound can be applied into the light emitting diode by using solution process and has very deep HOMO energy level. When the organic compound is applied into a chare transfer layer, a HOMO energy level bandgap between the charge transfer layer and an emitting material layer is reduced so that holes and electrons can be injected into the emitting material layer in a balanced manner.

COMPOUND, THIN FILM COMPRISING THE COMPOUND AND MENUFACTURING METHOD OF THE THIN FILM, AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE COMPOUND

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Paragraph 0116-0120, (2019/06/11)

In a compound, a thin film comprising the same, a method for manufacturing the thin film, and an organic light emitting device comprising the compound of the present invention, the compound of the present invention is represented by chemical formula 1. In the chemical formula 1, each of X_1, X_2, X_3, and X_4 independently represents hydrogen (H), aryl, diarylamine, or tert-butyl. A purpose of the present invention to provide the compound which contains a styrene group at the terminal thereof, has excellent solubility, and can be thermally cured at a low temperature.COPYRIGHT KIPO 2019

A carbazole di-aryl amines dendritic compound and its preparation method and application

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Paragraph 0054-0058, (2018/05/24)

The invention relates to a carbazole diarylamine dendritic compound as well as a preparation method and application of the carbazole diarylamine dendritic compound. According to the preparation method of the carbazole diarylamine dendritic compound, halogenated 9,9minute-spirobifluorene, a catalyst and a carbazole diarylamine compound are mixed with organic alkali; the mixture takes reaction under the inert gas protection by using xylene as a solvent; re-crystallization is performed for purification; the carbazole diarylamine dendritic compound obtained shown as the accompanying drawing is obtained. The prepared carbazole diarylamine dendritic compound has the advantages that the process and a refining method are simple and convenient; the carbazole diarylamine dendritic compound is very suitable for industrial production; better heat stability and better morphologic stability are realized; when the carbazole diarylamine dendritic compound is used as a hole-transporting material of a perovskite solar cell, higher photovoltaic conversion efficiency is realized.

Carbazolyltetraminepyrene hole transmission material and application thereof to perovskite solar cell

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Paragraph 0048-0052, (2018/06/26)

The invention discloses a carbazolyltetraminepyrene hole transmission material as well as preparation and application. A structural general formula of the carbazolyltetraminepyrene hole transmission material is shown as a formula I and a formula II. The carbazolyltetraminepyrene hole transmission material disclosed by the invention has good conjugate effect and good thermal stability; the energy grade of the carbazolyltetraminepyrene hole transmission material is matched with the energy grade of perovskite and has potential application value in the fields including perovskite solar cells and the like. The formula I and the formula II are shown in the description.

A two-benzofuran derivative and its preparation method and application

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Paragraph 0044; 0051-0053, (2017/08/25)

The invention relates to a derivative of dibenzofuran and a preparation method and application thereof. The preparation method of the derivative of the dibenzofuran comprises the steps that carbon-nitrogen coupling is performed on p-bromoanisole and p-methoxyaniline to obtain a first precursor; a two-step reaction is performed on the first precursor and 4,4'-dibromodiphenylamine protected by butyloxycarbonyl to obtain a second precursor, and a two-step reaction is performed on the first precursor and 3,6-dibromocarbazole protected by butyloxycarbonyl to obtain a third precursor; carbon-nitrogen coupling is performed on all the precursors and 2,8-dibromodibenzofuran under the action of a palladium catalyst to obtain the derivative of the dibenzofuran. The prepared derivative of the dibenzofuran is easy to synthesize, low in cost, high in glass transition temperature and good in heat stability, is a hole-transport material with the good properties and has the good effect when the derivative is applied to perovskite solar cells.

Two methoxyaniline-substituted dibenzofuran derivatives as hole-transport materials for perovskite solar cells

Shi, Yantao,Hou, Kaili,Wang, Yanxiang,Wang, Kai,Ren, HuiCai,Pang, MaoYin,Chen, Fan,Zhang, Sen

, p. 5415 - 5422 (2016/05/24)

2,2′,7,7′-Tetrakis(N,N-di-p-methoxyphenylamine)-9,9′-spirobifluorene (Spiro-OMeTAD), one of the classical organic photoelectric materials, has been widely used as a hole transport material (HTM) in perovskite solar cells (PSCs) due to its relatively higher conductivity, easier film formation, weak absorption in the visible region, etc. However, the complex synthesis process and the high synthesis cost of Spiro-OMeTAD severely limit the commercialization of this material. In this work, two economical methoxyaniline-substituted dibenzofuran derivatives, BF-002 and BF-003, are synthesized and successfully used as hole-transport materials in perovskite solar cells (PSCs). The important properties including light absorption, thermal stability, energy level, conductivity, as well as photovoltaic performance are systematically demonstrated. The highest power conversion efficiencies of the PSCs based on BF-002 and BF-003 are 14.20% and 14.07%, respectively, comparable to that of the PSCs based on Spiro-OMeTAD.

METHOD FOR PRODUCING CARBAZOLE COMPOUND HAVING TERTIARY AMINO GROUP, AND THE COMPOUND

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Paragraph 0063; 0066, (2018/11/03)

PROBLEM TO BE SOLVED: To provide a production method which can provide a carbazole compound having a tertiary amino group in high yield with suppressed formation of by-products, and which can simplify the production process. SOLUTION: The carbazole compound having a tertiary amino group is produced by using: a step of introducing a tertiary amino group into a compound comprising a 9-butoxycarbonylcarbazole structure; and a step of eliminating the butoxycarbonyl group from the compound. COPYRIGHT: (C)2016,JPOandINPIT

Pro-neurogenic compounds

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Page/Page column 155, (2015/09/22)

This invention relates generally to stimulating neurogenesis (e.g., post-natal neurogenesis, e.g., post-natal hippocampal neurogenesis) and protecting from neuron cell death.

Highly efficient soluble materials for blue phosphorescent organic light-emitting diode

Lee, Nam-Jin,Lee, Dae-Hee,Kim, Dong-Won,Lee, Ji-Hoon,Cho, Sang Hee,Jeon, Woo Sik,Kwon, Jang Hyuk,Suh, Min Chul

experimental part, p. 221 - 228 (2012/09/11)

A series of new carbazole derivatives with good solubility and electronic properties for use as host materials for blue phosphorescent organic light-emitting diodes is reported. A twisted biphenyl moiety at the center of the host materials was applied to

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