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4-(1-Pyrenyl)-N,N-bis[4-(1-pyrenyl)phenyl]benzenamine is a complex organic compound that belongs to the class of organic compounds known as biphenyls and derivatives. These compounds contain a structure made up of two benzene rings connected by a single covalent bond. This particular compound can be characterized by its chemical structure, which includes three pyrene moieties, which are polycyclic aromatic hydrocarbons containing four fused benzene rings, resulting in a flat aromatic system. It is used in various chemical research due to its unique properties. Its detailed properties such as melting point, boiling point, toxicity, and solubility may vary and are subject to the conditions and concentrations used in specific investigations. As with all chemicals, proper handling and adherence to safety protocols are necessary when dealing with 4-(1-Pyrenyl)-N,N-bis[4-(1-pyrenyl)phenyl]benzenamine.

349669-77-8

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349669-77-8 Usage

Uses

Used in Chemical Research:
4-(1-Pyrenyl)-N,N-bis[4-(1-pyrenyl)phenyl]benzenamine is used as a research compound for its unique properties in chemical studies. It is particularly valuable for investigations that require the synthesis and analysis of complex organic molecules with potential applications in various fields.
Used in Material Science:
In the field of material science, 4-(1-Pyrenyl)-N,N-bis[4-(1-pyrenyl)phenyl]benzenamine is used as a component in the development of new materials with specific properties. Its incorporation into materials can lead to advancements in areas such as electronics, photonics, and advanced materials for various applications.
Used in Pharmaceutical Development:
4-(1-Pyrenyl)-N,N-bis[4-(1-pyrenyl)phenyl]benzenamine is used as a potential candidate in the pharmaceutical industry for the development of new drugs. Its unique chemical structure may offer opportunities for the creation of novel therapeutic agents, particularly in the area of complex disease treatments that require targeted molecular interactions.
Used in Environmental Applications:
In environmental science, 4-(1-Pyrenyl)-N,N-bis[4-(1-pyrenyl)phenyl]benzenamine may be used as a tracer or indicator in studies related to environmental pollution and contamination. Its chemical properties could be harnessed to track the movement and effects of pollutants in the environment, aiding in the development of strategies for pollution control and remediation.

Check Digit Verification of cas no

The CAS Registry Mumber 349669-77-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,9,6,6 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 349669-77:
(8*3)+(7*4)+(6*9)+(5*6)+(4*6)+(3*9)+(2*7)+(1*7)=208
208 % 10 = 8
So 349669-77-8 is a valid CAS Registry Number.

349669-77-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-pyren-1-yl-N,N-bis(4-pyren-1-ylphenyl)aniline

1.2 Other means of identification

Product number -
Other names 4,4',4''-trispyrenylphenylamine

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:349669-77-8 SDS

349669-77-8Downstream Products

349669-77-8Relevant academic research and scientific papers

New core-pyrene π structure organophotocatalysts usable as highly efficient photoinitiators

Telitel, Sofia,Dumur, Frederic,Faury, Thomas,Graff, Bernadette,Tehfe, Mohamad-Ali,Gigmes, Didier,Fouassier, Jean-Pierre,Lalevee, Jacques

, p. 877 - 890 (2013)

Eleven di- and trifunctional compounds based on a core-pyrene π structure (Co-Py) were synthesized and investigated for the formation of free radicals. The application of two- and three-component photoinitiating systems (different Co-Pys with the addition of iodonium or sulfonium salts, alkyl halide or amine) was investigated in detail for cationic and radical photopolymerization reactions under near-UV-vis light. The proposed compounds can behave as new photocatalysts. Successful results in terms of rates of polymerization and final conversions were obtained. The strong MO coupling between the six different cores and the pyrene moiety was studied by DFT calculations. The different chemical intermediates are characterized by ESR and laser flash photolysis experiments. The mechanisms involved in the initiation step are discussed, and relationships between the core structure, the Co-Py absorption property, and the polymerization ability are tentatively proposed.

Distinct electroluminescent properties of triphenylamine derivatives in blue organic light-emitting devices

Lai, Shiu-Lun,Tong, Qing-Xiao,Chan, Mei-Yee,Ng, Tsz-Wai,Lo, Ming-Fai,Lee, Shuit-Tong,Lee, Chun-Sing

, p. 1206 - 1211 (2011)

Two highly fluorescent triphenylamines (TPA) end-capped respectively with one and three pyrene arms, namely N,N-diphenyl-4-(pyren-1-yl)aniline (PyTPA) and 4,4′,4′′-trispyrenylphenylamine (TPyPA), have been designed, synthesized and applied as hole-transpo

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