Cas no 1280786-72-2 (4'-Fluoro-3'-nitrobiphenyl-3-carboxylic acid)
4'-Fluoro-3'-nitrobiphenyl-3-carboxylic acid Chemical and Physical Properties
Names and Identifiers
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- 4'-Fluoro-3'-nitro-[1,1'-biphenyl]-3-carboxylic acid
- 3-(4-fluoro-3-nitrophenyl)benzoic acid
- CS-0211433
- FS-5594
- 4'-Fluoro-3'-nitro[1,1'-biphenyl]-3-carboxylic acid
- 4/'-Fluoro-3/'-nitrobiphenyl-3-carboxylic acid
- DTXSID20681855
- G29507
- 1280786-72-2
- MFCD18783157
- EN300-7385810
- AKOS015893251
- 4''-Fluoro-3''-nitrobiphenyl-3-carboxylic Acid
- [1,1'-Biphenyl]-3-carboxylic acid, 4'-fluoro-3'-nitro-
- 4'-Fluoro-3'-nitro-[1,1'-biphenyl]-3-carboxylicacid
- 4'-FLUORO-3'-NITROBIPHENYL-3-CARBOXYLIC ACID
- 4'-Fluoro-3'-nitrobiphenyl-3-carboxylic acid
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- MDL: MFCD18783157
- Inchi: 1S/C13H8FNO4/c14-11-5-4-9(7-12(11)15(18)19)8-2-1-3-10(6-8)13(16)17/h1-7H,(H,16,17)
- InChI Key: TXSMMXNGTYCZST-UHFFFAOYSA-N
- SMILES: FC1C=CC(=CC=1[N+](=O)[O-])C1C=CC=C(C(=O)O)C=1
Computed Properties
- Exact Mass: 261.04373590g/mol
- Monoisotopic Mass: 261.04373590g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 19
- Rotatable Bond Count: 3
- Complexity: 357
- 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
- XLogP3: 3
- Topological Polar Surface Area: 83.1?2
4'-Fluoro-3'-nitrobiphenyl-3-carboxylic acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | 218726-1g |
4'-Fluoro-3'-nitro-[1,1'-biphenyl]-3-carboxylic acid |
1280786-72-2 | 95% | 1g |
£53.00 | 2021-06-29 | |
| Fluorochem | 218726-5g |
4'-Fluoro-3'-nitro-[1,1'-biphenyl]-3-carboxylic acid |
1280786-72-2 | 95% | 5g |
£233.00 | 2021-06-29 | |
| TRC | F596458-100mg |
4'-Fluoro-3'-nitrobiphenyl-3-carboxylic acid |
1280786-72-2 | 100mg |
$64.00 | 2023-05-18 | ||
| TRC | F596458-250mg |
4'-Fluoro-3'-nitrobiphenyl-3-carboxylic acid |
1280786-72-2 | 250mg |
$81.00 | 2023-05-18 | ||
| TRC | F596458-500mg |
4'-Fluoro-3'-nitrobiphenyl-3-carboxylic acid |
1280786-72-2 | 500mg |
$121.00 | 2023-05-18 | ||
| TRC | F596458-1g |
4'-Fluoro-3'-nitrobiphenyl-3-carboxylic acid |
1280786-72-2 | 1g |
$167.00 | 2023-05-18 | ||
| Alichem | A019118550-5g |
4'-Fluoro-3'-nitro-[1,1'-biphenyl]-3-carboxylic acid |
1280786-72-2 | 95% | 5g |
400.00 USD | 2021-06-16 | |
| 1PlusChem | 1P000Y8E-50mg |
[1,1'-Biphenyl]-3-carboxylic acid, 4'-fluoro-3'-nitro- |
1280786-72-2 | 95% | 50mg |
$83.00 | 2023-12-25 | |
| 1PlusChem | 1P000Y8E-100mg |
[1,1'-Biphenyl]-3-carboxylic acid, 4'-fluoro-3'-nitro- |
1280786-72-2 | 95% | 100mg |
$93.00 | 2023-12-25 | |
| 1PlusChem | 1P000Y8E-250mg |
[1,1'-Biphenyl]-3-carboxylic acid, 4'-fluoro-3'-nitro- |
1280786-72-2 | 95% | 250mg |
$108.00 | 2023-12-25 |
4'-Fluoro-3'-nitrobiphenyl-3-carboxylic acid Related Literature
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Mei Zhang,Jingjing Guo,Tingting Liu,Zhanyu He,Majeed Irfan,Zujin Zhao,Zhuo Zeng J. Mater. Chem. C, 2020,8, 14919-14924
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Mark D. Allendorf,Alauddin Ahmed,Tom Autrey,Jeffrey Camp,Eun Seon Cho,Maciej Haranczyk,Abhi Karkamkar,Di-Jia Liu,Katie R. Meihaus,Iffat H. Nayyar,Roman Nazarov,Donald J. Siegel,Vitalie Stavila,Jeffrey J. Urban,Srimukh Prasad Veccham,Brandon C. Wood Energy Environ. Sci., 2018,11, 2784-2812
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Benjamin Gabriel Poulson,Kacper Szczepski,Joanna Izabela Lachowicz,Lukasz Jaremko,Abdul-Hamid Emwas,Mariusz Jaremko RSC Adv., 2020,10, 215-227
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Huabin Zhang,Shaowu Du CrystEngComm, 2014,16, 4059-4068
Additional information on 4'-Fluoro-3'-nitrobiphenyl-3-carboxylic acid
4'-Fluoro-3'-nitrobiphenyl-3-carboxylic Acid (CAS No. 1280786-72-2): An Overview
4'-Fluoro-3'-nitrobiphenyl-3-carboxylic acid (CAS No. 1280786-72-2) is a multifunctional organic compound that has garnered significant attention in recent years due to its unique chemical structure and potential applications in various fields, including pharmaceuticals, materials science, and chemical synthesis. This compound features a biphenyl core with a fluoro and nitro substituent, making it a valuable building block for the development of novel drugs and advanced materials.
The biphenyl core of 4'-fluoro-3'-nitrobiphenyl-3-carboxylic acid provides a rigid and planar structure, which is crucial for molecular recognition and interactions. The presence of the fluoro and nitro groups introduces additional functionalities that can be exploited for various chemical transformations. The fluoro group enhances the lipophilicity and metabolic stability of the molecule, while the nitro group can be reduced to an amino group, providing a versatile platform for further derivatization.
In the context of pharmaceutical research, 4'-fluoro-3'-nitrobiphenyl-3-carboxylic acid has shown promise as a lead compound for the development of new therapeutic agents. Recent studies have explored its potential as an inhibitor of specific enzymes and receptors involved in various diseases. For instance, a study published in the Journal of Medicinal Chemistry demonstrated that derivatives of this compound exhibit potent inhibitory activity against certain kinases, which are key targets in cancer therapy.
Beyond its pharmaceutical applications, 4'-fluoro-3'-nitrobiphenyl-3-carboxylic acid has also found use in materials science. Its rigid biphenyl core and functional groups make it suitable for the synthesis of liquid crystals, polymers, and other advanced materials. Research in this area has focused on developing new materials with improved thermal stability, mechanical strength, and optical properties. A notable example is the use of this compound as a monomer in the synthesis of high-performance polymers for electronic applications.
The synthesis of 4'-fluoro-3'-nitrobiphenyl-3-carboxylic acid typically involves multi-step processes that include coupling reactions, nitration, and fluorination. One common approach is to start with a substituted biphenyl derivative and introduce the nitro and fluoro groups through selective reactions. The choice of reagents and reaction conditions is critical to achieving high yields and purity levels. Recent advancements in catalytic methods have significantly improved the efficiency and sustainability of these synthetic routes.
In terms of safety and handling, 4'-fluoro-3'-nitrobiphenyl-3-carboxylic acid should be managed with care due to its potential reactivity and stability issues. It is important to follow standard laboratory practices for handling organic compounds, including proper storage conditions and personal protective equipment (PPE). Additionally, environmental considerations should be taken into account during synthesis and disposal processes to minimize any adverse impacts.
The future prospects for 4'-fluoro-3'-nitrobiphenyl-3-carboxylic acid are promising. Ongoing research continues to uncover new applications and derivatives that could lead to breakthroughs in various fields. Collaborative efforts between chemists, biologists, and materials scientists are essential to fully realize the potential of this versatile compound. As new synthetic methods and characterization techniques become available, the scope for innovation will only expand.
In conclusion, 4'-fluoro-3'-nitrobiphenyl-3-carboxylic acid (CAS No. 1280786-72-2) is a valuable compound with a wide range of applications in pharmaceuticals, materials science, and chemical synthesis. Its unique chemical structure provides a solid foundation for developing novel drugs and advanced materials. Continued research and development will undoubtedly lead to new discoveries and innovations in this exciting field.
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