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2,7-Dibromo-9-vinyl-9H-carbazole is a chemical compound characterized by a molecular formula of C16H10Br2N. It is a carbazole derivative distinguished by the presence of two bromine atoms and a vinyl group attached to the 9th position of the carbazole ring. 2,7-Dibromo-9-vinyl-9H-carbazole is notable for its unique structure and properties, which make it a valuable asset in various scientific and industrial applications.

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  • 1438252-33-5 Structure
  • Basic information

    1. Product Name: 2,7-Dibromo-9-vinyl-9H-carbazole
    2. Synonyms: 2,7-Dibromo-9-vinyl-9H-carbazole;2,7-dibromo-9-ethenyl-9H-carbazole
    3. CAS NO:1438252-33-5
    4. Molecular Formula: C14H9Br2N
    5. Molecular Weight: 351.03596
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 1438252-33-5.mol
  • Chemical Properties

    1. Melting Point: 130 °C
    2. Boiling Point: 428.6±38.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.69±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,7-Dibromo-9-vinyl-9H-carbazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,7-Dibromo-9-vinyl-9H-carbazole(1438252-33-5)
    11. EPA Substance Registry System: 2,7-Dibromo-9-vinyl-9H-carbazole(1438252-33-5)
  • 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: 1438252-33-5(Hazardous Substances Data)

1438252-33-5 Usage

Uses

Used in Organic Synthesis:
2,7-Dibromo-9-vinyl-9H-carbazole is utilized as a key intermediate in organic synthesis for the creation of complex organic molecules. Its versatile reactivity allows for the development of a wide range of chemical products.
Used in Material Science:
In the field of material science, 2,7-Dibromo-9-vinyl-9H-carbazole is used as a component in the fabrication of advanced materials. Its unique structure contributes to the properties of these materials, enhancing their performance.
Used in Organic Light-Emitting Diodes (OLEDs):
2,7-Dibromo-9-vinyl-9H-carbazole is employed as a material in the construction of organic light-emitting diodes due to its electronic and optical properties, which are crucial for the efficient functioning of OLEDs.
Used in Photoconductive Materials:
2,7-Dibromo-9-vinyl-9H-carbazole is also used in the development of photoconductive materials, where its ability to conduct electricity upon exposure to light is leveraged for various applications.
Used in Pharmaceuticals:
2,7-Dibromo-9-vinyl-9H-carbazole has been studied for its potential use in pharmaceuticals, indicating that it may have properties that could be beneficial in the development of new drugs or drug delivery systems.
Used in Building Blocks for Complex Organic Molecules:
As a building block, 2,7-Dibromo-9-vinyl-9H-carbazole is used in the synthesis of complex organic molecules, where its structural features can be integrated into larger molecular frameworks to achieve specific chemical or physical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 1438252-33-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,8,2,5 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1438252-33:
(9*1)+(8*4)+(7*3)+(6*8)+(5*2)+(4*5)+(3*2)+(2*3)+(1*3)=155
155 % 10 = 5
So 1438252-33-5 is a valid CAS Registry Number.

1438252-33-5Downstream Products

1438252-33-5Relevant articles and documents

Iridium-Catalyzed Vinylation of Carbazole Derivatives with Vinyl Acetate

Kimura, Jungo,Nakamichi, Seiya,Ogawa, Shinji,Obora, Yasushi

, p. 719 - 723 (2017)

We report a practical method for the synthesis of vinylcarbazoles via iridium-catalyzed vinylation of carbazoles with vinyl acetate as the vinyl source. This simple and efficient reaction using an iridium catalyst provides a convenient method for producing monomers for the synthesis of poly(N-vinylcarbazole)s, which are used in electroluminescent devices.

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