1028647-93-9 Usage
Description
3-(4-bromophenyl)-N-phenylcarbazole is a white crystalline powder that serves as a valuable research chemical. It is a derivative of carbazole, a heterocyclic organic compound with a tricyclic structure, and features a bromophenyl group attached to the 4-position of the phenyl ring.
Uses
Used in Research and Development:
3-(4-bromophenyl)-N-phenylcarbazole is used as a research chemical for the development of new compounds and materials. Its unique structure and properties make it a promising candidate for various applications in the fields of chemistry and materials science.
Used in Organic Synthesis:
In the field of organic synthesis, 3-(4-bromophenyl)-N-phenylcarbazole is used as a building block or intermediate for the synthesis of more complex organic molecules. Its reactivity and functional groups can be exploited to create a wide range of compounds with potential applications in various industries.
Used in Pharmaceutical Research:
3-(4-bromophenyl)-N-phenylcarbazole is also used in pharmaceutical research as a potential lead compound for the development of new drugs. Its unique structure and properties may offer novel therapeutic opportunities, and further research is needed to explore its potential in this area.
Used in Material Science:
In material science, 3-(4-bromophenyl)-N-phenylcarbazole can be used as a component in the development of new materials with specific properties. Its incorporation into polymers, for example, may result in materials with improved stability, conductivity, or other desirable characteristics.
Overall, 3-(4-bromophenyl)-N-phenylcarbazole is a versatile research chemical with potential applications in various fields, including organic synthesis, pharmaceutical research, and material science. Its unique structure and properties make it a valuable tool for scientists and researchers working to develop new compounds and materials with innovative properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1028647-93-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,8,6,4 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1028647-93:
(9*1)+(8*0)+(7*2)+(6*8)+(5*6)+(4*4)+(3*7)+(2*9)+(1*3)=159
159 % 10 = 9
So 1028647-93-9 is a valid CAS Registry Number.
1028647-93-9Relevant articles and documents
Tertiary amine derivatives and organic electroluminescent device including the same
-
Paragraph 0156-0158, (2021/06/01)
A UV-region high-energy external light source is effectively absorbed to minimize damage to organic materials in the organic electroluminescent device. 1 Is a cross-sectional view of an organic electroluminescence device according to the present invention. O-2 electrode 1 Or more organic material layers disposed between the (2) and (1) th electrodes. A capping layer is included. The organic material layer and/or the capping layer may include the 1 st amine derivative represented by Formula 3. Chemical Formula 1. Wherein each substituent in Formula 1 is as defined in the description of the invention.
Asymmetric triarylamine
-
Paragraph 0043; 0046; 0047, (2021/01/11)
The invention discloses asymmetric triarylamine, relates to the technical field of preparation of organic materials, and aims to reduce the crystallinity of molecules and improve the film-forming property of the molecules by eliminating the symmetry of the molecules so as to solve the problem that the crystallinity of a common triarylamine material on the market influences the performance of a device at present.
COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND A ELECTRONIC DEVICE THEREOF
-
Paragraph 0097; 0101; 0110; 0111, (2020/06/24)
The present invention provides a novel compound capable of improving luminance efficiency, stability, and service life of an element, an organic electronic element using the same, and an electronic device thereof. By using the compound of the present invention, high luminance efficiency, low driving voltage, and high heat resistance of the element can be achieved, and color purity and service life of the element can be greatly improved.