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9-Benzyl-2,7-dibromo-9H-carbazole is a chemical compound belonging to the carbazole family, characterized by the presence of two bromine atoms at the 2 and 7 positions of the carbazole ring and a benzyl group attached at the 9 position. This unique structural feature endows it with potential applications in organic synthesis, materials science, and possibly pharmaceuticals.

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  • 1384281-49-5 Structure
  • Basic information

    1. Product Name: 9-Benzyl-2,7-dibromo-9H-carbazole
    2. Synonyms: 9-Benzyl-2,7-dibromo-9H-carbazole;9-Benzyl-2,7-dibromo-9H-carbazole
    3. CAS NO:1384281-49-5
    4. Molecular Formula: C19H13Br2N
    5. Molecular Weight: 415.12122
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1384281-49-5.mol
  • Chemical Properties

    1. Melting Point: 161.0 to 165.0 °C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: 9-Benzyl-2,7-dibromo-9H-carbazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9-Benzyl-2,7-dibromo-9H-carbazole(1384281-49-5)
    11. EPA Substance Registry System: 9-Benzyl-2,7-dibromo-9H-carbazole(1384281-49-5)
  • 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: 1384281-49-5(Hazardous Substances Data)

1384281-49-5 Usage

Uses

Used in Organic Synthesis:
9-Benzyl-2,7-dibromo-9H-carbazole serves as a valuable building block for the synthesis of various organic compounds and materials with specific properties and functions. Its unique structure allows for the creation of new molecules with tailored characteristics for different applications.
Used in Materials Science:
In the field of materials science, 9-Benzyl-2,7-dibromo-9H-carbazole can be utilized to develop materials with specific functionalities. Its structural attributes make it a candidate for creating advanced materials with potential uses in various industries.
Used in Pharmaceutical Applications:
9-Benzyl-2,7-dibromo-9H-carbazole may exhibit interesting biological activities that warrant further exploration for potential pharmaceutical applications. Its unique chemical structure could lead to the development of new drugs or therapeutic agents.
Used in Research and Development:
9-Benzyl-2,7-dibromo-9H-carbazole is also valuable in research and development settings, where its properties can be studied and harnessed to advance scientific understanding and innovation in chemistry and related fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1384281-49-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,2,8 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1384281-49:
(9*1)+(8*3)+(7*8)+(6*4)+(5*2)+(4*8)+(3*1)+(2*4)+(1*9)=175
175 % 10 = 5
So 1384281-49-5 is a valid CAS Registry Number.

1384281-49-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-Benzyl-2,7-dibromo-9H-carbazole

1.2 Other means of identification

Product number -
Other names -(5-Carboxypentyl)biotinamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1384281-49-5 SDS

1384281-49-5Downstream Products

1384281-49-5Relevant articles and documents

CARBAZOLE COMPOUND HAVING ANTI-VIRUS ACTIVITY

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Paragraph 0182; 0183; 0184; 0247; 0248, (2018/03/25)

The present invention relates to a carbazole compound having anti-virus activity, and more particularly, to a novel compound selected from the group of consisting of a carbazole compound which shows excellent anti-proliferative efficacy against hepatitis C virus (HCV), a pharmaceutically acceptable salt thereof, a hydrate thereof, and an isomer thereof; an anti-virus pharmaceutical composition including the novel compound as an active ingredient; a pharmaceutical composition for preventing or treating liver diseases caused by hepatitis C virus; and a method of preparing the novel compound.

Novel efficient hole-transporting materials based on a 1,1′-bi-2-naphthol core for perovskite solar cells

Qiao, Wenhua,Chen, Yu,Li, Fusheng,Zong, Xueping,Sun, Zhe,Liang, Mao,Xue, Song

, p. 482 - 492 (2017/01/12)

New star-shaped and efficient hole-transporting materials based on a 1,1′-bi-2-naphthol central core for perovskite solar cells are developed via facile synthesis. The 1,1′-bi-2-naphthol is first applied into the field of perovskite solar cells. The 2,7-carbazole-bis(4-methoxy-phenyl)-amine and 3,6-carbazole-bis(4-methoxy-phenyl)-amine are used as end groups. A reference compound based on a 3,3′-biphenyl core is prepared as well. The new materials have suitable highest occupied molecular orbital levels to match well with the valence band of CH3NH3PbI3, and they all exhibit a glass transition temperature higher than 160 °C. A device fabricated by hole-transporting materials based on 1,1′-bi-2-naphthol and 2,7-carbazole-bis(4-methoxy-phenyl)-amine in conjunction with a carbon counter electrode achieves the highest power conversion efficiency of 8.38% under the illumination of 100 mW cm?2, which is comparable to that fabricated by commercial spiro-OMeTAD (8.73%). Dark current, IPCE and IMVS measurements are also discussed. The introduction of 2,7-carbazole-bis(4-methoxy-phenyl)-amine onto the 1,1′-bi-2-naphthol central core tends to enhance Jsc of a device, and 3,6-carbazole-bis(4-methoxy-phenyl)-amine improves Voc. This work provides a new series of hole-transporting materials to fabricate economic and efficient perovskite solar cells.

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