Cas no 880800-19-1 (N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diamine)
N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diamine Chemical and Physical Properties
Names and Identifiers
-
- N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diamine
- 1,4-Benzenediamine,N4-[1,1'-biphenyl]-4-yl-N1,N1-diphenyl-
- 4-N,4-N-diphenyl-1-N-(4-phenylphenyl)benzene-1,4-diamine
- 1,4-Benzenediamine, N′-[1,1′-biphenyl]-4-yl-N,N-diphenyl- (9CI)
- N4-[1,1′-Biphenyl]-4-yl-N1,N1-diphenyl-1,4-benzenediamine (ACI)
- N4-{[1,1'-BIPHENYL]-4-YL}-N1,N1-DIPHENYLBENZENE-1,4-DIAMINE
- 880800-19-1
- MFCD09878766
- BS-50611
- N-Biphenyl-4-yl-N',N'-diphenyl-benzene-1,4-diamine
- DTXSID90650639
- AKOS015853721
- Q-102383
- N-Biphenyl-4-yl-N' pound notN'-diphenyl-benzene-1 pound not4-diamine
- DB-012557
- CS-0099495
- N1-([1,1'-Biphenyl]-4-yl)-N4,N4-diphenylbenzene-1,4-diamine
- N~4~-([1,1'-Biphenyl]-4-yl)-N~1~,N~1~-diphenylbenzene-1,4-diamine
- SCHEMBL2180914
-
- MDL: MFCD09878766
- Inchi: 1S/C30H24N2/c1-4-10-24(11-5-1)25-16-18-26(19-17-25)31-27-20-22-30(23-21-27)32(28-12-6-2-7-13-28)29-14-8-3-9-15-29/h1-23,31H
- InChI Key: BMWFGSBSRCFWTA-UHFFFAOYSA-N
- SMILES: C1C=CC(C2C=CC(NC3C=CC(N(C4C=CC=CC=4)C4C=CC=CC=4)=CC=3)=CC=2)=CC=1
Computed Properties
- Exact Mass: 412.19400
- Monoisotopic Mass: 412.194
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 32
- Rotatable Bond Count: 6
- Complexity: 495
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 15.3A^2
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: 8.3
Experimental Properties
- Density: 1.172
- Boiling Point: 593.2°C at 760 mmHg
- Flash Point: 202.3°C
- Refractive Index: 1.687
- PSA: 15.27000
- LogP: 8.64000
N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diamine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM185990-25g |
N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diamine |
880800-19-1 | 95+% | 25g |
$478 | 2021-06-16 | |
| Alichem | A019086804-25g |
N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diamine |
880800-19-1 | 97% | 25g |
$516.11 | 2023-08-31 | |
| Chemenu | CM185990-25g |
N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diamine |
880800-19-1 | 95+% | 25g |
$478 | 2022-05-27 | |
| abcr | AB283617-250 mg |
N-Biphenyl-4-yl-N',N'-diphenyl-benzene-1,4-diamine; . |
880800-19-1 | 250 mg |
€113.20 | 2023-07-20 | ||
| abcr | AB283617-1 g |
N-Biphenyl-4-yl-N',N'-diphenyl-benzene-1,4-diamine; . |
880800-19-1 | 1 g |
€193.60 | 2023-07-20 | ||
| abcr | AB283617-5 g |
N-Biphenyl-4-yl-N',N'-diphenyl-benzene-1,4-diamine; . |
880800-19-1 | 5 g |
€517.00 | 2023-07-20 | ||
| Fluorochem | 036955-1g |
N-Biphenyl-4-yl-N',N'-diphenyl-benzene-1,4-diamine |
880800-19-1 | 97% | 1g |
£57.00 | 2022-03-01 | |
| Fluorochem | 036955-5g |
N-Biphenyl-4-yl-N',N'-diphenyl-benzene-1,4-diamine |
880800-19-1 | 97% | 5g |
£169.00 | 2022-03-01 | |
| Fluorochem | 036955-25g |
N-Biphenyl-4-yl-N',N'-diphenyl-benzene-1,4-diamine |
880800-19-1 | 97% | 25g |
£591.00 | 2022-03-01 | |
| eNovation Chemicals LLC | D544056-1g |
N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diaMine |
880800-19-1 | 97% | 1g |
$170 | 2024-05-24 |
N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diamine Related Literature
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Cheng Fang,Jinjian Wu,Zahra Sobhani,Md. Al Amin,Youhong Tang Anal. Methods, 2019,11, 163-170
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Juan J. Sánchez,Miguel López-Haro,Juan C. Hernández-Garrido,Ginesa Blanco,Miguel A. Cauqui,José M. Rodríguez-Izquierdo,José A. Pérez-Omil,José J. Calvino,María P. Yeste J. Mater. Chem. A, 2019,7, 8993-9003
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Andre Prates Pereira,Tao Dong,Eric P. Knoshaug,Nick Nagle,Ryan Spiller,Bonnie Panczak,Christopher J. Chuck,Philip T. Pienkos Sustainable Energy Fuels, 2020,4, 3400-3408
Additional information on N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diamine
N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diamine (CAS No. 880800-19-1): A High-Performance Organic Compound for Advanced Applications
N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diamine (CAS No. 880800-19-1) is a specialized organic compound that has garnered significant attention in recent years due to its unique chemical structure and versatile applications. This compound, often referred to as a triarylamine derivative, belongs to the class of aromatic amines, which are widely used in materials science, electronics, and advanced manufacturing.
The molecular structure of N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diamine features a central benzene ring substituted with biphenyl and diphenylamine groups. This arrangement imparts exceptional electron-transport properties and thermal stability, making it highly valuable for applications in organic light-emitting diodes (OLEDs), photovoltaic devices, and electroluminescent materials. Researchers and industry professionals are increasingly exploring its potential in next-generation flexible electronics and energy-efficient displays, aligning with the global push toward sustainable technologies.
One of the most notable characteristics of N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diamine is its ability to function as a hole-transport material (HTM) in optoelectronic devices. This property is critical for improving the efficiency of solar cells and OLED screens, which are in high demand due to the growing consumer electronics market. Recent advancements in green chemistry have also highlighted its role in reducing the environmental impact of electronic waste, a key concern among environmentally conscious consumers.
In addition to its electronic applications, N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diamine has shown promise in catalysis and polymer science. Its robust aromatic framework allows it to serve as a building block for high-performance polymers, which are used in aerospace, automotive, and medical device manufacturing. The compound's high thermal resistance and chemical inertness make it particularly suitable for demanding industrial environments.
The synthesis of N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diamine typically involves multi-step organic reactions, including Ullmann coupling and Buchwald-Hartwig amination. These methods ensure high purity and yield, which are essential for commercial applications. As the demand for high-efficiency electronic materials grows, manufacturers are investing in scalable production techniques to meet industry needs.
From a market perspective, the compound is gaining traction due to its compatibility with emerging technologies such as wearable electronics and Internet of Things (IoT) devices. Companies specializing in advanced materials are actively researching ways to integrate N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diamine into next-gen products, capitalizing on its superior performance characteristics.
In summary, N-Biphenyl-4-yl-N',N'-diphenylbenzene-1,4-diamine (CAS No. 880800-19-1) represents a cutting-edge solution for modern technological challenges. Its applications in optoelectronics, polymer science, and sustainable manufacturing position it as a key player in the future of material innovation. As research continues to uncover new uses for this compound, its relevance in high-tech industries is expected to grow exponentially.
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