Cas no 105112-76-3 (4,4'-Bis(3-aminophenoxy)biphenyl)
4,4'-Bis(3-aminophenoxy)biphenyl Chemical and Physical Properties
Names and Identifiers
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- M-TOLIDINE
- 2,2'-DIMETHYL-4,4'-DIAMINOBIPHENYL
- APB-144
- 1’-Biphenyl]-4,4’-diamine,2,2’-dimethyl-[1
- 2,2’-dimethylbenzidine
- 4-(4-amino-2-methylphenyl)-3-methylbenzenamine
- 4,4'-Diamino-2,2'-dimethylbiphenyl
- 4,4-bis(3-aminophenoxy)biphenyl
- 2,2'-dimethyl[1,1'-biphenyl]-4,4'-diamine
- 3,3 [1,1-biphenyl]-4,4-doil bi(oxy)-bisbenzamine
- 4,4-BIS(3-AMINOPHENOXY)BIPHENYL(43BAPOBP)
- 3-[1-(3-aminophenoxy)-4-phenylcyclohexa-2,4-dien-1-yl]oxyaniline
- 4,4'-Bis(3-aminophenoxy)biphenyl
- I06-1441
- 3,3'-(Biphenyl-4,4'-diylbis(oxy))dianiline
- FT-0655660
- AS-11797
- CS-0378037
- DTXSID70668237
- SCHEMBL203512
- 3,3'-[[1,1'-Biphenyl]-4,4'-diylbis(oxy)]bis[benzenamine]
- EC 700-102-1
- E79398
- 3,3'-([1,1'-Biphenyl]-4,4'-diylbis(oxy))dianiline
- 4,4-BIS(3-AMINOPHENOXY)BIPHENYL (BAPB-M)
- 3-{4-[4-(3-aminophenoxy)phenyl]phenoxy}aniline
- AKOS025311131
- UCQABCHSIIXVOY-UHFFFAOYSA-N
- MFCD00357502
- 105112-76-3
- 3,3'-[[1,1'-biphenyl]-4,4'-diyl-bis-(oxy)]-bis-benzeneamine
- 3-[4-[4-(3-aminophenoxy)phenyl]phenoxy]aniline
- A801151
- 3,3a(2)-[[1,1a(2)-Biphenyl]-4,4a(2)-diylbis(oxy)]bis[benzenamine]
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- MDL: MFCD00357502
- Inchi: 1S/C24H20N2O2/c25-19-3-1-5-23(15-19)27-21-11-7-17(8-12-21)18-9-13-22(14-10-18)28-24-6-2-4-20(26)16-24/h1-16H,25-26H2
- InChI Key: UCQABCHSIIXVOY-UHFFFAOYSA-N
- SMILES: O(C1C=CC=C(C=1)N)C1C=CC(=CC=1)C1C=CC(=CC=1)OC1C=CC=C(C=1)N
Computed Properties
- Exact Mass: 368.15200
- Monoisotopic Mass: 212.131
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 28
- Rotatable Bond Count: 5
- Complexity: 205
- 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: 52A^2
- XLogP3: 5.2
Experimental Properties
- Density: 1.226
- Melting Point: 105-106 °C
- Boiling Point: 344.4 °C at 760 mmHg
- Flash Point: 192.9 °C
- Refractive Index: 1.638
- PSA: 70.50000
- LogP: 7.26500
4,4'-Bis(3-aminophenoxy)biphenyl Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | B405558-10mg |
4,4'-Bis(3-aminophenoxy)biphenyl |
105112-76-3 | 10mg |
$ 50.00 | 2022-06-07 | ||
| TRC | B405558-50mg |
4,4'-Bis(3-aminophenoxy)biphenyl |
105112-76-3 | 50mg |
$ 95.00 | 2022-06-07 | ||
| TRC | B405558-100mg |
4,4'-Bis(3-aminophenoxy)biphenyl |
105112-76-3 | 100mg |
$ 160.00 | 2022-06-07 | ||
| Alichem | A019108570-5g |
3,3'-([1,1'-Biphenyl]-4,4'-diylbis(oxy))dianiline |
105112-76-3 | 95% | 5g |
$899.94 | 2023-09-04 | |
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | B6326-5G |
4,4'-Bis(3-aminophenoxy)biphenyl |
105112-76-3 | >98.0%(T)(HPLC) | 5g |
¥2990.00 | 2024-04-18 | |
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | B6326-25G |
4,4'-Bis(3-aminophenoxy)biphenyl |
105112-76-3 | >98.0%(T)(HPLC) | 25g |
¥5990.00 | 2024-04-18 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1448707-5g |
4,4'-Bis(3-aminophenoxy)biphenyl |
105112-76-3 | 95+% | 5g |
¥3996.00 | 2024-08-09 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1448707-25g |
4,4'-Bis(3-aminophenoxy)biphenyl |
105112-76-3 | 95+% | 25g |
¥8618.00 | 2024-08-09 | |
| Aaron | AR008RXT-5g |
4,4-BIS(3-AMINOPHENOXY)BIPHENYL(43BAPOBP) |
105112-76-3 | 98% | 5g |
$409.00 | 2023-12-16 | |
| Aaron | AR008RXT-25g |
4,4-BIS(3-AMINOPHENOXY)BIPHENYL(43BAPOBP) |
105112-76-3 | 98% | 25g |
$323.00 | 2025-02-10 |
4,4'-Bis(3-aminophenoxy)biphenyl Suppliers
4,4'-Bis(3-aminophenoxy)biphenyl Related Literature
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A. B. F. da Silva,K. Capelle Phys. Chem. Chem. Phys., 2009,11, 4564-4569
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4. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198
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M. Zeiger,N. J?ckel,P. Strubel,L. Borchardt,R. Reinhold,W. Nickel,J. Eckert,V. Presser,S. Kaskel J. Mater. Chem. A, 2015,3, 17983-17990
Additional information on 4,4'-Bis(3-aminophenoxy)biphenyl
Recent Advances in the Application of 4,4'-Bis(3-aminophenoxy)biphenyl (CAS: 105112-76-3) in Chemical Biology and Pharmaceutical Research
4,4'-Bis(3-aminophenoxy)biphenyl (CAS: 105112-76-3) has emerged as a compound of significant interest in chemical biology and pharmaceutical research due to its unique structural properties and versatile applications. This aromatic diamine compound, characterized by its biphenyl core and flexible ether linkages, has demonstrated remarkable potential in polymer synthesis, drug delivery systems, and as a building block for advanced materials. Recent studies have explored its role in enhancing the thermal stability and mechanical properties of polyimide films, while other investigations have focused on its utility in developing novel drug carriers with improved biocompatibility.
In the field of polymer chemistry, researchers have utilized 4,4'-Bis(3-aminophenoxy)biphenyl as a key monomer for synthesizing high-performance polyimides. A 2023 study published in the Journal of Polymer Science demonstrated that polyimides derived from this monomer exhibited exceptional thermal stability (up to 500°C) and mechanical strength, making them suitable for aerospace and microelectronics applications. The study highlighted how the compound's molecular structure contributes to enhanced chain packing and intermolecular interactions, resulting in materials with superior properties compared to conventional polyimides.
Pharmaceutical applications of 4,4'-Bis(3-aminophenoxy)biphenyl have gained attention in recent drug development research. Its amine functional groups allow for facile conjugation with various therapeutic agents, as evidenced by a 2024 Nature Communications publication describing its use in creating pH-responsive drug delivery systems. The research team successfully developed nanoparticles that could release anticancer drugs selectively in tumor microenvironments, demonstrating improved therapeutic efficacy and reduced side effects in preclinical models. This approach leverages the compound's ability to form stable yet responsive linkages with drug molecules.
Emerging research has also explored the biological activity of 4,4'-Bis(3-aminophenoxy)biphenyl derivatives. A recent Bioorganic & Medicinal Chemistry study (2024) reported that certain structural analogs of this compound exhibited promising inhibitory activity against specific protein kinases involved in inflammatory pathways. While the parent compound itself shows limited direct biological activity, these findings suggest that careful structural modifications could yield novel therapeutic candidates targeting various disease pathways.
From a synthetic chemistry perspective, advances in the production and purification of 4,4'-Bis(3-aminophenoxy)biphenyl have been notable. A 2023 Chemical Engineering Journal article detailed an improved catalytic process for its synthesis, achieving higher yields (85-90%) and purity (>99.5%) while reducing environmental impact. These process improvements are particularly significant given the growing industrial demand for high-purity monomers in specialty polymer production.
Looking forward, researchers anticipate expanding applications of 4,4'-Bis(3-aminophenoxy)biphenyl in biomaterials and nanotechnology. Preliminary studies suggest its potential in creating self-assembling nanostructures for biomedical imaging and tissue engineering. However, challenges remain in fully characterizing its long-term biocompatibility and optimizing its performance in various applications. Continued research in these areas will be crucial for translating laboratory findings into practical, commercial applications across multiple industries.
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