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69386-35-2

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69386-35-2 Usage

General Description

9H-Carbazole, 2,7-bis(1,1-dimethylethyl)- is a chemical compound that belongs to the class of carbazoles, which are aromatic heterocyclic compounds. It is commonly used in the synthesis of various organic molecules and is also known for its photophysical properties, making it suitable for applications in optoelectronic devices such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The presence of the 2,7-bis(1,1-dimethylethyl) groups in the carbazole structure enhances its stability and can also influence its electronic and optical properties. Overall, this chemical compound has broad potential applications in the field of organic electronics and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 69386-35-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,8 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69386-35:
(7*6)+(6*9)+(5*3)+(4*8)+(3*6)+(2*3)+(1*5)=172
172 % 10 = 2
So 69386-35-2 is a valid CAS Registry Number.

69386-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,7-di-tert-butylcarbazole

1.2 Other means of identification

Product number -
Other names 2,7-di-tert-butyl-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:69386-35-2 SDS

69386-35-2Relevant articles and documents

Solution spraying OLED (Organic Light-Emitting Diode) material

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Paragraph 0079; 0080; 0081; 0108-0110, (2016/10/10)

The invention discloses a series of solution spraying OLED (Organic Light-Emitting Diode) materials. The structures of the materials are shown in formula I. The materials shown in the formula I have the characteristics of being easily soluble in an organic solvent and good in the heat stability, are applied to preparing lighting equipment by modes of fluid manufacturing processes such as print, instilling, coating, printing and the like. An organic light-emitting device prepared by utilizing the materials through a coating method has the characteristics that the power efficiency is good, the material utilization is high, the manufacturing cost of the organic light-emitting device is greatly reduced, material synthesis and purification methods are simple, the materials are suitable for large scale production, and the like, and are ideal selections of light-emitting materials of the organic light-emitting device. The application of organic light emitting diode materials as host materials in an luminescent layer or doped materials or independent light-emitting materials or hole-transport materials or electron transport materials is in the scope of protection. The chemical formula is shown in the description.

CATALYST SYSTEMS FOR OLEFIN POLYMERIZATION

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, (2015/11/18)

The instant invention provides procatalysts and catalyst systems for olefin polymerization, olefin based polymers polymerized therewith, and process for producing the same. In one embodiment, the instant invention provides a procatalyst comprising a metal

Triphenylphosphine-mediated reductive cyclization of 2-nitrobiphenyls: A practical and convenient synthesis of carbazoles

Freeman, Adam W.,Urvoy, Marie,Criswell, Megan E.

, p. 5014 - 5019 (2007/10/03)

The synthesis of a series of substituted carbazoles from the corresponding 2-nitrobiphenyl derivatives using a novel modification of the Cadogan reaction is described. Cyclization of the 2-nitrobiphenyls was achieved via reductive deoxygenation of the nitro groups using a slight excess of triphenylphosphine in a suitable solvent. We have observed a temperature dependence on the extent of conversion under these conditions, with higher boiling solvents affording higher yields across a range of substrates. The new reaction conditions are very straightforward and convenient to execute, tolerate a broad range of functional groups, and yield carbazole products in the absence of unwanted side products.

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