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255829-30-2

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255829-30-2 Usage

General Description

4-(3,6-di-tert-butyl-9H-carbazol-9-yl)benzenamine, also known as 2-(3,6-di-tert-butyl-9H-carbazol-9-yl)aniline, is an organic compound with the molecular formula C32H37N. It is a derivative of carbazole, a tricyclic aromatic compound, and it contains a benzene ring attached to an aniline group and a carbazole moiety. This chemical is commonly used in the synthesis of organic semiconductors and optoelectronic materials due to its unique electronic and optical properties. Its 3,6-di-tert-butyl substituents provide steric protection and enhance its stability and solubility in organic solvents, making it a valuable building block in the development of advanced materials for a variety of electronic and photonic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 255829-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,5,8,2 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 255829-30:
(8*2)+(7*5)+(6*5)+(5*8)+(4*2)+(3*9)+(2*3)+(1*0)=162
162 % 10 = 2
So 255829-30-2 is a valid CAS Registry Number.

255829-30-2Relevant articles and documents

Novel symmetric purpurine compound and preparation method and applications thereof

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Paragraph 0041-0042; 0049, (2020/03/09)

The invention discloses a novel symmetric purpurine compound, which is composed of an acceptor 4,4'-dipyridine, different donor groups, and different counter anions. The structure of the compound is shown in the description. The invention also discloses a

Micromolecular hole transport material applied to solution processing type organic light-emitting device

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Paragraph 0040-0041; 0044, (2019/07/01)

The invention relates to a micromolecular hole transport material applied to a solution processing type organic electroluminescent device. The micromolecular hole transport material is prepared according to the following steps: adding a planar N heterocyclic ring and 4-fluoronitrobenzene into a reaction bottle according to a molar ratio of 1:1 to 1:1.5 with DMF as a solvent and K2CO3 as an acid binding agent, and conducting reacting at 100-120 DEG C for 5-10 hours to obtain a nitro compound; and reducing the obtained nitro compound by using SnCl2.H2O in a molar ratio of 1:2 to 1: 3, and carrying out a reflux reaction in ethanol for 4-6 hours. The end group of the micromolecular hole transport material is a planar N-heterocycle. The hole transport material with an end group of a planar N heterocyclic ring and capable of being processed in a solution can be applied to the fields of organic electroluminescent devices, and also can be applied to the fields of organic solar cells, organic thin film transistors or organic photoreceptors.

Efficient and straightforward click synthesis of structurally related dendritic triazoles

Mangione,Spanevello,Anzardi

, p. 47681 - 47688 (2017/10/23)

A simple, rapid and efficient copper-catalyzed 1,3-dipolar cycloaddition reaction is described for the synthesis of a novel family of twelve triazolic dendrimers structurally related. The products were the result of the click reaction of three cores and four different azides in tetrahydrofuran applying a homogeneous copper catalysis. The reaction intermediates and products were obtained in very good to excellent yields using straightforward and simple work-up procedures. This new family of compounds contain electroactive moieties such as carbazole and triphenylamine which may turn them into excellent candidates for the development of optoelectronic organic materials.

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