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9-phenyl-9H,9'H-2,3'-bicarbazole is a chemical compound characterized by its molecular formula C24H16N2. It presents as a pale yellow powder with a molecular weight of 332.396 g/mol. 9-phenyl-9H,9'H-2,3'-bicarbazole is distinguished by its unique chemical structure and high thermal stability, which are pivotal for its applications in the realm of organic electronics.

1382955-10-3

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1382955-10-3 Usage

Uses

Used in Organic Electronics Industry:
9-phenyl-9H,9'H-2,3'-bicarbazole is utilized as a hole transport material for its critical role in the performance of organic light-emitting diodes (OLEDs). Its ability to efficiently transport holes contributes to the improved functionality and efficiency of these devices.
9-phenyl-9H,9'H-2,3'-bicarbazole is also used as a hole transport material in organic photovoltaic (OPV) devices, where its properties enhance the conversion of light into electricity, thereby boosting the overall performance of the solar cells.
Research is ongoing to explore the potential of 9-phenyl-9H,9'H-2,3'-bicarbazole in other areas such as electroluminescent materials, which could further expand its applications in display technologies, and organic semiconductors, where it may contribute to the development of new electronic and optoelectronic devices.

Check Digit Verification of cas no

The CAS Registry Mumber 1382955-10-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,2,9,5 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1382955-10:
(9*1)+(8*3)+(7*8)+(6*2)+(5*9)+(4*5)+(3*5)+(2*1)+(1*0)=183
183 % 10 = 3
So 1382955-10-3 is a valid CAS Registry Number.

1382955-10-3Downstream Products

1382955-10-3Relevant articles and documents

CARBAZOLE BASED COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

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Paragraph 0187-0189; 0196-0198, (2018/02/21)

The present specification provides a carbazole-based compound represented by chemical formula 1, and an organic light-emitting device comprising the same. According to one embodiment of the present specification, the compound may be used as a material for an organic material layer in an organic light-emitting device to improve efficiency, lower driving voltage, and/or improve lifetime characteristics of the device. Additionally, another embodiment of the present specification provides an organic light-emitting device which comprises: a first electrode; a second electrode disposed to face the first electrode; and one or more organic material layers disposed between the first electrode and the second electrode, wherein at least one of the organic layer materials comprises a compound represented by the chemical formula 1.COPYRIGHT KIPO 2017

Material for organic electroluminescence device and organic electroluminescence device

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Page/Page column 135; 136; 155, (2016/05/02)

A material for organic electroluminescence device having a specific central skeleton to which a cyano-substituted aromatic hydrocarbon group or a cyano-substituted heterocyclic group is bonded at its specific position is described. Further described is an organic electroluminescence device including an organic thin film layer between an anode and a cathode. The organic thin film layer include an light emitting layer and at least one layer of the organic thin film layer contains the material for organic electroluminescence device. The material for organic electroluminescence device realizes an organic electroluminescence device with good emission efficiency.

nitrogen-containing polycyclic compound and an organic electroluminescent device including the same

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, (2016/10/09)

Disclosed are a nitrogen-containing polycyclic compound and an organic electroluminescent device including the same.

ORGANIC ELECTROLUMINESCENT COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME

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Paragraph 210; 211; 212, (2015/11/23)

The present disclosure relates to an organic electroluminescent compound of Formula 1 (variables R1 -R10 defined herein), and an organic electroluminescent device comprising the same. By using the organic electroluminescent compound according to the present disclosure, it is possible to produce an organic electroluminescent device which can be operated at a lowered driving voltage, shows excellence in luminous efficiency such as current efficiency and power efficiency, and has high color purity and improved lifespan. [Formula should be entered here]

A NOVEL COMBINATION OF A HOST COMPOUND AND A DOPANT COMPOUND AND AN ORGANIC ELECTROLUMINESCENCE DEVICE COMPRISING THE SAME

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Paragraph 140; 141; 146; 147; 182; 183, (2014/01/17)

The present invention relates to a specific combination of a dopant compound and a host compound, and an organic electroluminescent device comprising the same. The organic electroluminescent device of the present invention provides the advantages of excellent luminous characteristics with lower driving voltages, compared to devices using conventional luminescent materials.

NOVEL ORGANIC ELECTROLUMINESCENT COMPOUNDS AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME

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, (2013/11/18)

The present invention relates to a novel organic electroluminescent compound and an organic electroluminescent device comprising the same. The organic electroluminescent compound according to the present invention has high green luminous efficiency and superior material lifespan characteristics, compared with conventional phosphorescent host materials, and thus can provide an organic electroluminescent device which is excellent in operational lifespan, and induces increased power efficiency and improves power consumption.

AROMATIC HETEROCYCLE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT ELEMENT USING SAME

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Paragraph 0161; 0162, (2013/12/02)

An aromatic heterocyclic derivative represented by the following formula (1)-1 or (1)-2: wherein in the formula (1)-1 or (1)-2, A is a substituted or unsubstituted nitrogen-containing heterocyclic group including 2 to 30 ring carbon atoms; B is a substituted or unsubstituted aromatic hydrocarbon group including 6 to 30 ring carbon atoms or a substituted or unsubstituted aromatic heterocyclic group including 2 to 30 ring carbon atoms; n is an integer of 2 or more; and Czs are independently an aromatic heterocyclic group including a predetermined structure.

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