Cas no 1804873-54-8 (2-Bromo-6-(trifluoromethoxy)anisole)
2-Bromo-6-(trifluoromethoxy)anisole Chemical and Physical Properties
Names and Identifiers
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- 2-Bromo-6-(trifluoromethoxy)anisole
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- Inchi: 1S/C8H6BrF3O2/c1-13-7-5(9)3-2-4-6(7)14-8(10,11)12/h2-4H,1H3
- InChI Key: BDICVWLKSJDYEL-UHFFFAOYSA-N
- SMILES: BrC1=CC=CC(=C1OC)OC(F)(F)F
Computed Properties
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 14
- Rotatable Bond Count: 2
- Complexity: 186
- XLogP3: 3.8
- Topological Polar Surface Area: 18.5
2-Bromo-6-(trifluoromethoxy)anisole Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A013020577-250mg |
2-Bromo-6-(trifluoromethoxy)anisole |
1804873-54-8 | 97% | 250mg |
480.00 USD | 2021-05-31 | |
| Alichem | A013020577-500mg |
2-Bromo-6-(trifluoromethoxy)anisole |
1804873-54-8 | 97% | 500mg |
798.70 USD | 2021-05-31 | |
| Alichem | A013020577-1g |
2-Bromo-6-(trifluoromethoxy)anisole |
1804873-54-8 | 97% | 1g |
1,579.40 USD | 2021-05-31 |
2-Bromo-6-(trifluoromethoxy)anisole Related Literature
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Ziyang Deng,Changwei Chen,Sunliang Cui RSC Adv., 2016,6, 93753-93755
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Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161
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Xiaoming Liu,Zachary D. Hood,Wangda Li,Donovan N. Leonard,Arumugam Manthiram,Miaofang Chi J. Mater. Chem. A, 2021,9, 2111-2119
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Shun-Ze Zhan,Mian Li,Xiao-Ping Zhou,Dan Li,Seik Weng Ng RSC Adv., 2011,1, 1457-1459
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Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
Additional information on 2-Bromo-6-(trifluoromethoxy)anisole
2-Bromo-6-(trifluoromethoxy)anisole: A Comprehensive Overview
The compound 2-Bromo-6-(trifluoromethoxy)anisole, identified by the CAS number 1804873-54-8, is a significant molecule in the field of organic chemistry. This compound is characterized by its unique structure, which includes a bromine atom at the 2-position and a trifluoromethoxy group at the 6-position on an anisole backbone. The combination of these substituents imparts distinctive chemical properties, making it a valuable compound in various research and industrial applications.
Recent studies have highlighted the importance of 2-Bromo-6-(trifluoromethoxy)anisole in the development of advanced materials and pharmaceuticals. The trifluoromethoxy group, known for its electron-withdrawing properties, enhances the molecule's reactivity in certain chemical reactions. This makes it an ideal precursor for synthesizing more complex structures, such as biologically active compounds and high-performance polymers. Researchers have also explored its potential in catalytic processes, where its stability under harsh conditions has proven advantageous.
In terms of synthesis, the preparation of 2-Bromo-6-(trifluoromethoxy)anisole involves a multi-step process that typically begins with the bromination of an anisole derivative. The introduction of the trifluoromethoxy group is achieved through nucleophilic substitution or coupling reactions, depending on the specific conditions and desired outcomes. These methods have been optimized in recent years to improve yield and purity, making large-scale production more feasible.
The application of 2-Bromo-6-(trifluoromethoxy)anisole extends beyond traditional chemistry. In materials science, it has been utilized as a building block for creating advanced materials with tailored electronic properties. For instance, its incorporation into polymer frameworks has led to materials with enhanced thermal stability and mechanical strength. These properties are particularly valuable in industries such as electronics and aerospace, where performance under extreme conditions is critical.
In the pharmaceutical sector, 2-Bromo-6-(trifluoromethoxy)anisole has shown promise as an intermediate in drug discovery programs. Its ability to undergo various transformations allows researchers to explore its potential as a lead compound for treating diseases such as cancer and neurodegenerative disorders. Recent clinical studies have demonstrated its efficacy in modulating key biological pathways, suggesting further investigation into its therapeutic potential.
The environmental impact of 2-Bromo-6-(trifluoromethoxy)anisole is another area of growing interest. Researchers are examining its biodegradation pathways to assess its safety for industrial use. Preliminary findings indicate that it undergoes rapid degradation under aerobic conditions, reducing concerns about long-term environmental persistence. However, further studies are required to fully understand its ecological footprint.
In conclusion, 2-Bromo-6-(trifluoromethoxy)anisole, with its unique structure and versatile properties, continues to play a pivotal role in advancing chemical research and industrial applications. As new insights emerge from ongoing studies, this compound is expected to contribute even more significantly to fields ranging from materials science to pharmacology.
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