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9-(4-Bromophenyl)-2-phenyl-Carbazole is a carbazole derivative with the molecular formula C26H17BrN. It features a bromo-substituted phenyl group at the 9-position and a phenyl group at the 2-position. This chemical compound is known for its high thermal stability and electron-transporting properties, which make it a promising candidate for various applications in the field of organic electronics.

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  • 1235563-74-2 Structure
  • Basic information

    1. Product Name: 9-(4-Bromophenyl)-2-phenyl-Carbazole
    2. Synonyms: 9-(4-Bromophenyl)-2-phenyl-Carbazole
    3. CAS NO:1235563-74-2
    4. Molecular Formula: C24H16BrN
    5. Molecular Weight: 398.29454
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1235563-74-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 9-(4-Bromophenyl)-2-phenyl-Carbazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9-(4-Bromophenyl)-2-phenyl-Carbazole(1235563-74-2)
    11. EPA Substance Registry System: 9-(4-Bromophenyl)-2-phenyl-Carbazole(1235563-74-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1235563-74-2(Hazardous Substances Data)

1235563-74-2 Usage

Uses

Used in Organic Electronic Devices:
9-(4-Bromophenyl)-2-phenyl-Carbazole is used as a component in organic light-emitting diodes (OLEDs) for its ability to enhance device performance and stability. Its electron-transporting properties contribute to the efficient operation of OLEDs, leading to improved brightness and longer device lifetimes.
Used in Organic Photovoltaics:
In the field of organic photovoltaics, 9-(4-Bromophenyl)-2-phenyl-Carbazole is utilized as a material to improve the efficiency and stability of solar cells. Its electron-transporting capabilities play a crucial role in the conversion of light into electricity, making it a valuable component in the development of next-generation solar technologies.
Used in Optoelectronics and Semiconductor Applications:
9-(4-Bromophenyl)-2-phenyl-Carbazole is used as a material in the development of new optoelectronic devices and semiconductor technologies. Its unique molecular structure and electronic properties allow for the creation of innovative materials with enhanced performance characteristics, such as higher sensitivity, faster response times, and improved energy efficiency.
Further research and development of 9-(4-Bromophenyl)-2-phenylcarbazole could lead to advancements in the field of organic electronics, opening up new possibilities for applications in various industries, including display technology, energy harvesting, and communication systems.

Check Digit Verification of cas no

The CAS Registry Mumber 1235563-74-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,5,5,6 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1235563-74:
(9*1)+(8*2)+(7*3)+(6*5)+(5*5)+(4*6)+(3*3)+(2*7)+(1*4)=152
152 % 10 = 2
So 1235563-74-2 is a valid CAS Registry Number.

1235563-74-2Downstream Products

1235563-74-2Relevant articles and documents

N-Arylation of carbazole by microwave-assisted ligand-free catalytic CuI reaction

Kwon, Jae Kwan,Cho, Joong Hyun,Ryu, Young-Sil,Oh, Se Hwan,Yum, Eul Kgun

experimental part, p. 4820 - 4825 (2011/07/31)

N-Arylation of carbazole has been achieved in high yields within 1 h using a microwave-assisted catalytic CuI reaction with no organic ligand. The N-arylation can be performed by various arylhalides, such as phenyl, pyridine, thiophene, and thiazole moieties. Specifically, N-arylated bromocarbazoles were converted into useful synthetic intermediates for functionalized carbazole materials.

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