122215-84-3

Basic information

• Product Name: N-[1,1-biphenyl]-4-yl-N-phenyl-[1,1-Biphenyl]-4-amine
• Synonyms: N-[1,1-biphenyl]-4-yl-N-phenyl-[1,1-Biphenyl]-4-amine;[1,1'-Biphenyl]-4-amine, N-[1,1'-biphenyl]-4-yl-N-phenyl-;N-Phenyl-N,N-bis(biphenyl-4-yl)amine;N,N-Bis(4-biphenylyl)aniline;N,N-Bis(4-biphenylyl)aniline
• CAS NO: 122215-84-3
• Molecular Formula: C₃₀H₂₃N
• Molecular Weight: 397.51032
• Mol File: 122215-84-3.mol

Chemical Properties

• Melting Point: 169.0 to 173.0 °C
• Boiling Point: 583.2±39.0 °C(Predicted)
• Appearance: /
• Density: 1.131±0.06 g/cm3(Predicted)
• PKA: -3.14±0.50(Predicted)
• CAS DataBase Reference: N-[1,1-biphenyl]-4-yl-N-phenyl-[1,1-Biphenyl]-4-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-[1,1-biphenyl]-4-yl-N-phenyl-[1,1-Biphenyl]-4-amine(122215-84-3)
• EPA Substance Registry System: N-[1,1-biphenyl]-4-yl-N-phenyl-[1,1-Biphenyl]-4-amine(122215-84-3)

Safety Data

• Hazardous Substances Data: 122215-84-3(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
N-[1,1-biphenyl]-4-yl-N-phenyl-[1,1-Biphenyl]-4-amine is used as a building block in organic synthesis for the creation of more complex molecules. Its presence of biphenyl groups and an amine functional group allows for versatile chemical reactions and the formation of a wide range of compounds.
Used in Pharmaceutical Research and Drug Development:
Due to its unique structure and properties, N-[1,1-biphenyl]-4-yl-N-phenyl-[1,1-Biphenyl]-4-amine may be utilized in pharmaceutical research and drug development as a potential candidate for the design of new drugs. Its biphenyl and amine components could contribute to the development of novel therapeutic agents with specific pharmacological properties.
Used in Chemical Research:
N-[1,1-biphenyl]-4-yl-N-phenyl-[1,1-Biphenyl]-4-amine is also used in chemical research to study the properties and reactivity of biphenyl and amine groups. Understanding the behavior of this compound in various chemical reactions can provide insights into the development of new synthetic methods and the creation of new materials.

Upstream product

• 591-50-4 iodobenzene 
• 102113-98-4 bis(biphenyl-4-yl)amine 
• 1591-31-7 4-iodo-biphenyl 
• 62-53-3 aniline 
• 92-66-0 4-bromo-1,1'-biphenyl 
• 32228-99-2 4-phenyldiphenylamine 
• 2051-62-9 4'-biphenyl chloride 
• 108-86-1 bromobenzene 

Downstream Products

• 499128-71-1 N-([1′,1′-biphenyl]-4-yl)-N-(4-bromophenyl)-[1,1′-biphenyl]-4-amine 
• 915031-02-6 N,N-di([1,1‘-biphenyl]-4-yl)-4’-chloro-[1,1’-biphenyl]-4-amine 

Relevant articles and documents

Organic light-emitting material containing triazine group and aniline group, application as well as device

The invention belongs to the field of preparation and application science and technology of organic light-emitting materials, and particularly relates to an organic light-emitting material containingtriazine group and aniline group and a preparation method thereof, application as well as a device. The organic light-emitting material provided by the invention takes triazine and benzidine as cores,and has excellent heat stability so as to be beneficial to the improvement of efficiency and stability of the device, has high fluorescence quantum yield to be used as a light-emitting guest materialand has good dual polarity to be used as a light-emitting host material.

COMPOUND AND ORGANIC ELECTRONIC DEVICE USING THE SAME

Provided are a novel compound and an organic electronic device using the same. The novel compound is represented by the following Formula (I):

Polycarbazole compd., manufacturing method thereof, and use thereof

PROBLEM TO BE SOLVED: To provide a novel carbazole compound with a high T1, a production method thereof and a use thereof.SOLUTION: A carbazole compound represented by general formula (1) is used for any one or more layer of a light emitting layer, a hole transport layer and a hole injection layer of an organic EL element, where Arand Arindependently represent a 6-40C aryl group or a 3-40C heteroaryl group or the like.

A new compound and an organic light emitting element including the same

The present invention relates to a novel compound and an organic light emitting device comprising the same. The compound according to the present invention may be used as hole injection, hole transport, electron injection and transport, and light emitting materials in an organic light emitting device, and the organic light emitting device according to the present invention has excellent properties in terms of efficiency, driving voltage, and life-span.

CARBAZOLE DERIVATIVE, AND LIGHT-EMITTING ELEMENT, LIGHT-EMITTING DEVICE, AND ELECTRONIC DEVICE USING CARBAZOLE DERIVATIVE

To provide a light-emitting element having high luminous efficiency and to provide a light-emitting device and an electronic device which consumes low power and is driven at low voltage, a carbazole derivative represented by the general formula (1) is provided. In the formula, α1, α2, α3, and α4 each represent an arylene group having less than or equal to 13 carbon atoms; Ar1 and Ar2 each represent an aryl group having less than or equal to 13 carbon atoms; R1 represents any of a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted phenyl group, and a substituted or unsubstituted biphenyl group; and R2represents any of an alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted phenyl group, and a substituted or unsubstituted biphenyl group. In addition, l, m, and n are each independenly 0 or 1.

Evaluation of aromatic amination catalyzed by palladium on carbon: A practical synthesis of triarylamines

A heterogeneous palladium on carbon (Pd/C)-catalyzed coupling between amines and aromatic halides including aromatic chlorides has been achieved using sodium tert-butoxide (NaO-t-Bu) and 1,1′-bis(diphenylphosphino)ferrocene (dppf) as a ligand in cyclopentyl methyl ether (CPME). The use of potassium tert-butoxide (KO-t-Bu) in place of NaO-t-Bu brought about the benzyne-mediated aromatic amination even without Pd/C and dppf, giving a mixture of regioisomers when 4-substituted bromobenzenes were employed as the substrate. The combination of Pd/C, dppf, NaO-t-Bu could be utilized for the syntheses of a broad range of triarylamines by replacing CPME with mesitylene which can provide a higher reaction temperature. The Pd/C could be quantitatively recovered and reused until at least the fourth cycle without any loss in catalytic activity. The quite low leaching of palladium (1.1%) was demonstrated by an inductively coupled plasma-atomic emission spectrometric analysis.