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3,6-bis(9-phenyl-9H-carbazol-3-yl)-9H-carbazole is a complex chemical compound characterized by its multiple carbazole units. It is distinguished by its high thermal stability, good film-forming properties, and efficient charge transport capabilities, which are attributed to its carbazole core structure. This structure also endows the compound with excellent electron-donating properties, making it a suitable candidate for use in optoelectronic devices. Its unique molecular structure and electronic properties render it a promising material for various applications within the realm of organic electronics.

1060735-19-4

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1060735-19-4 Usage

Uses

Used in Organic Light-Emitting Diodes (OLEDs):
3,6-bis(9-phenyl-9H-carbazol-3-yl)-9H-carbazole is used as a hole-transporting material in OLEDs for its high thermal stability and efficient charge transport capabilities. 3,6-bis(9-phenyl-9H-carbazol-3-yl)-9H-carbazole's electron-donating properties, derived from its carbazole core, are crucial for the performance of these optoelectronic devices.
Used in Optoelectronic Devices:
In the optoelectronic industry, 3,6-bis(9-phenyl-9H-carbazol-3-yl)-9H-carbazole is utilized for its unique molecular structure and electronic properties, which make it a promising material for the development of advanced devices that require efficient charge transport and thermal stability.
While the provided materials do not specify other industries or applications, the compound's properties suggest potential uses in various fields where high thermal stability, efficient charge transport, and good film-forming properties are required. Further research and development could reveal additional applications in areas such as solar cells, sensors, or other electronic devices.

Check Digit Verification of cas no

The CAS Registry Mumber 1060735-19-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,0,7,3 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1060735-19:
(9*1)+(8*0)+(7*6)+(6*0)+(5*7)+(4*3)+(3*5)+(2*1)+(1*9)=124
124 % 10 = 4
So 1060735-19-4 is a valid CAS Registry Number.

1060735-19-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-bis(9-phenylcarbazol-3-yl)carbazole

1.2 Other means of identification

Product number -
Other names 9,9''-diphenyl-3,3':6',3'-ter(9H-carbazole)

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:1060735-19-4 SDS

1060735-19-4Relevant academic research and scientific papers

Small molecule material based on naphtho-indene fluorine two-photon absorption and preparation method of small molecule material

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Paragraph 0059; 0060; 0061; 0062, (2018/10/19)

The invention discloses a small molecule material based on naphtho-indene fluorine high two-photon absorption and a preparation method of the small molecule material. The small molecule material is mainly characterized in that a multielement conjugated condensed ring structure-naphtho-indene fluorine unit is adopted as a core, and an organic small molecule fluorescence material with intense two-photon response can be prepared by selecting different acceptor electron units. The material is a naphtho-indene fluorine unit small molecule compound with C-C coupling and C-N coupling. The small molecule material disclosed by the invention has the characteristics of intense single/two-photon florescence intensity, good solubleness and the like, and has great application prospects in biological fields such as two-photon fluorescence imaging, two-photon fluorescence microscope, two-photon fluorescence probes, and the like.

Organic Electroluminescent materials and devices

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Page/Page column 117; 118, (2016/08/07)

Novel tricarbazole compounds are provided. By appropriately selecting the nature of the tricarbazole substituents, compounds with appropriate HOMO and LUMO energies can be obtained for use as materials in a secondary hole transport layer.

NITROGEN-CONTAINING AROMATIC HETEROCYCLIC DERIVATIVE AND ORGANIC ELECTROLUMINESCENCE DEVICE USING SAME

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, (2013/07/31)

A nitrogen-containing aromatic heterocyclic derivative represented by the following formula, wherein X1 to X3 are a single bond, CRaRb, NRc, an oxygen atom or a sulfur atom, and when all of X1 to X3 is a single bond, at least one of Ara, Arb and Arc is an aryl group having 6 to 20 ring carbon atoms substituted with a heteroaryl group, an aryloxy group or a heteroaryloxy group, or a substituted or unsubstituted heteroaryl group having 5 to 20 ring atoms.

SECONDARY HOLE TRANSPORTING LAYER WITH TRICARBAZOLE COMPOUNDS

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Page/Page column, (2013/09/26)

Novel tricarbazole compounds are provided. By appropriately selecting the nature of the tricarbazole substituents, compounds with appropriate HOMO and LUMO energies can be obtained for use as materials in a secondary hole transport layer.

Organic compound, anthracene derivative, and light-emitting element, light-emitting device, and electronic device using anthracene derivative

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Page/Page column 276, (2008/12/08)

Objects of the present invention are to provide novel anthracene derivatives and novel organic compounds; a light-emitting element that has high emission efficiency; a light-emitting element that is capable of emitting blue light with high luminous efficiency; a light-emitting element that is capable of operation for a long time; and a light-emitting device and an electronic device that have lower power consumption. An anthracene derivative represented by a general formula (1) and an organic compound represented by a general formula (17) are provided. A light-emitting element that has high emission efficiency can be obtained by use of the anthracene derivative represented by the general formula (1). Further, a light-emitting element that has a long life can be obtained by use of the anthracene derivative represented by the general formula (1).

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