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1,1'-(2,2'-Dimethyl-[1,1'-biphenyl]-4,4'-diyl)bis(3,6-dimethyl-9H-carbazole) is a complex organic compound with the molecular formula C70H62N2. It features a biphenyl core linked to two 3,6-dimethyl-9H-carbazole groups, which may contribute to its potential applications in various fields.

1262783-41-4

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1262783-41-4 Usage

Uses

Used in Organic Electronics:
1,1'-(2,2'-Dimethyl-[1,1'-biphenyl]-4,4'-diyl)bis(3,6-dimethyl-9H-carbazole) is used as a semiconductor material for its potential applications in the field of organic electronics. Its unique structure and properties make it a candidate for further exploration and development in this industry.
Used in Optoelectronic Devices:
In the Optoelectronics Industry, 1,1'-(2,2'-Dimethyl-[1,1'-biphenyl]-4,4'-diyl)bis(3,6-dimethyl-9H-carbazole) is used as a component in the development of optoelectronic devices due to its photophysical properties, which are crucial for light interaction and emission.
Used in Organic Light-Emitting Diodes (OLEDs):
1,1'-(2,2'-Dimethyl-[1,1'-biphenyl]-4,4'-diyl)bis(3,6-dimethyl-9H-carbazole) is utilized as a material in OLEDs for its ability to enhance the performance of these devices, contributing to improved light emission and efficiency.
Used in Organic Solar Cells:
In the Renewable Energy Industry, specifically within the domain of organic solar cells, 1,1'-(2,2'-Dimethyl-[1,1'-biphenyl]-4,4'-diyl)bis(3,6-dimethyl-9H-carbazole) is used as a component to improve the efficiency and performance of solar energy conversion, capitalizing on its semiconductor characteristics.
Other Industrial and Research Applications:
1,1'-(2,2'-Dimethyl-[1,1'-biphenyl]-4,4'-diyl)bis(3,6-dimethyl-9H-carbazole) may also have potential uses in other industries and research areas, although further investigation is necessary to fully comprehend its capabilities and optimize its application.

Check Digit Verification of cas no

The CAS Registry Mumber 1262783-41-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,7,8 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1262783-41:
(9*1)+(8*2)+(7*6)+(6*2)+(5*7)+(4*8)+(3*3)+(2*4)+(1*1)=164
164 % 10 = 4
So 1262783-41-4 is a valid CAS Registry Number.

1262783-41-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4-[4-(3,6-dimethyl-9H-carbazol-1-yl)-2-methylphenyl]-3-methylphenyl]-3,6-dimethyl-9H-carbazole

1.2 Other means of identification

Product number -
Other names -

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:1262783-41-4 SDS

1262783-41-4Downstream Products

1262783-41-4Relevant academic research and scientific papers

A series of CBP-derivatives as host materials for blue phosphorescent organic light-emitting diodes

Schroegel, Pamela,Tomkeviciene, Ausra,Strohriegl, Peter,Hoffmann, Sebastian T.,Koehler, Anna,Lennartz, Christian

, p. 2266 - 2273 (2011)

We report a series of CBP-derivatives with superior thermal and electronic properties for the use as host materials for blue electrophosphorescent organic light emitting diodes. We applied a systematic variation of the substitution pattern in the 2- and 2′-position of the biphenyl unit and the 3- and 6-position of the carbazole moieties. In contrast to the crystalline parent compound CBP, all methyl and trifluoromethyl substituted derivatives show amorphous behaviour. Substitution in the 2- and 2′-position of the biphenyl causes a twisting of the phenyl rings. Hence, the degree of conjugation of the molecules is limited which leads to enlarged triplet energies of approximately 2.95 eV compared to 2.58 eV for CBP. The methyl substitution at the active 3- and 6-position of the pendant carbazole units yields materials with an electrochemically stable behaviour against oxidation. The Royal Society of Chemistry.

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