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9-[3-(Dibenzo[b,d]furan-2-yl)phenyl]-9H-carbazole is a complex chemical compound that features a carbazole core fused with a dibenzo[b,d]furan-2-yl group. 9-[3-(Dibenzo[b,d]furan-2-yl)phenyl]-9H-carbazole is characterized by its unique molecular structure, which combines the properties of a colorless crystalline carbazole, known for its use in polymer and dye synthesis, with the aromatic characteristics of a dibenzo[b,d]furan-2-yl moiety, a polycyclic aromatic hydrocarbon. The fusion of these elements suggests a wide range of potential applications in materials science, organic synthesis, and as a precursor for the development of innovative organic materials. Its distinctive structural and chemical attributes render 9-[3-(Dibenzo[b,d]furan-2-yl)phenyl]-9H-carbazole a compound of significant interest for further exploration and industrial application.

1338446-77-7

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1338446-77-7 Usage

Uses

Used in Materials Science:
9-[3-(Dibenzo[b,d]furan-2-yl)phenyl]-9H-carbazole is used as a component in the development of advanced materials due to its unique structural properties that may enhance material characteristics such as stability, conductivity, or light absorption.
Used in Organic Synthesis:
As an intermediate in organic synthesis, 9-[3-(Dibenzo[b,d]furan-2-yl)phenyl]-9H-carbazole is utilized for the creation of a variety of organic compounds, leveraging its reactive sites for further functionalization and the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
9-[3-(Dibenzo[b,d]furan-2-yl)phenyl]-9H-carbazole is used as a building block in the design and synthesis of pharmaceutical compounds, potentially contributing to the development of new drugs with novel therapeutic properties.
Used in Dye and Pigment Industry:
Given its carbazole core, 9-[3-(Dibenzo[b,d]furan-2-yl)phenyl]-9H-carbazole is used as a precursor in the production of dyes and pigments, where its molecular structure may impart specific color characteristics and stability to the final products.
Used in Research and Development:
9-[3-(Dibenzo[b,d]furan-2-yl)phenyl]-9H-carbazole serves as a subject of research for scientists exploring new chemical reactions, material properties, and potential applications in various fields, including nanotechnology and advanced chemical engineering.

Check Digit Verification of cas no

The CAS Registry Mumber 1338446-77-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,4,4 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1338446-77:
(9*1)+(8*3)+(7*3)+(6*8)+(5*4)+(4*4)+(3*6)+(2*7)+(1*7)=177
177 % 10 = 7
So 1338446-77-7 is a valid CAS Registry Number.

1338446-77-7SDS

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-[3-(dibenzo[b,d]furan-2-yl)phenyl]-9H-carbazole

1.2 Other means of identification

Product number -
Other names CzDBF

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:1338446-77-7 SDS

1338446-77-7Downstream Products

1338446-77-7Relevant academic research and scientific papers

The effect of the substitution position of dibenzofuran on the photophysical and charge-transport properties of host materials for phosphorescent organic light-emitting diodes

Lee, Chil Won,Seo, Jeong-A,Gong, Myoung-Seon,Lee, Jun Yeob

, p. 1194 - 1198 (2013)

A twist in the tail: The effect of varying the substitution position of dibenzofuran on its photophysical properties and organic light-emitting diode device performance was systematically investigated by synthesizing three compounds with 2-, 3- and 4-substitution patterns (see scheme). The proper selection of substitution position can control the photophysical properties and performance of the materials. Copyright

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