Cas no 69403-12-9 (2-Fluoro-4-(trifluoromethyl)aniline)
2-Fluoro-4-(trifluoromethyl)aniline Chemical and Physical Properties
Names and Identifiers
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- l-phenylalanine dehydrogenase
- L-Phenylalanine Dehydrogenase from Rhodococcus spec. M4
- L-PHENYLALANINE DEHYDROGENASE FROM SPOROSARCINA SP LARGER THAN 6 U MG
- Phenylalanine dehydrogenase
- 2-fluoro-4-(trifluoromethyl)aniline
- 4-Amino-3-fluorobenzotrifluoride
- 3-FLUORO-4-AMINOBENZOTRIFLUORIDE
- 2-fluoro-4-trifluoromethylaniline
- Benzenamine, 2-fluoro-4-(trifluoromethyl)-
- 2-FLUORO-4-(TRIFLUOROMETHYL)BENZENAMINE
- 2-fluoro-4-(trifluoromethyl)phenylamine
- 2-FLUORO-4-(TRIFLUORMETHYL)ANILINE
- 4-Amino-3-fluorobenzotri-fluoride
- PubChem2813
- 2-(Benzoyloxymethyl)benzoicacid
- a,a,a,2-Tetrafluoro-p-toluidine
- Fluoro-4-(trifluoromethyl)aniline
- WT395
- 2-f
- 2-Fluoro-4-(trifluoromethyl)aniline
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- Inchi: 1S/C7H5F4N/c8-5-3-4(7(9,10)11)1-2-6(5)12/h1-3H,12H2
- InChI Key: ARHDUOQIXLGANT-UHFFFAOYSA-N
- SMILES: FC1=C(C=CC(C(F)(F)F)=C1)N
Computed Properties
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 12
- Rotatable Bond Count: 0
- Complexity: 156
- XLogP3: 2.2
- Topological Polar Surface Area: 26
2-Fluoro-4-(trifluoromethyl)aniline Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | L920305-50U |
L-PHENYLALANINE DEHYDROGENASE |
69403-12-9 | 50U |
¥5,737.50 | 2022-01-10 |
2-Fluoro-4-(trifluoromethyl)aniline Suppliers
2-Fluoro-4-(trifluoromethyl)aniline Related Literature
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Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
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Li-Hua Gan,Rui Wu,Jian-Lei Tian,Patrick W. Fowler Phys. Chem. Chem. Phys., 2017,19, 419-425
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3. An all-solid-state imprinted polymer-based potentiometric sensor for determination of bisphenol S?Rongning Liang,Tanji Yin,Ruiqing Yao,Wei Qin RSC Adv., 2016,6, 73308-73312
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Kanjun Sun,Fengting Hua,Shuzhen Cui,Yanrong Zhu,Hui Peng,Guofu Ma RSC Adv., 2021,11, 37631-37642
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Haitao Li,Yu Pan,Zhizhi Wang,Shan Chen,Ruixin Guo,Jianqiu Chen RSC Adv., 2015,5, 100775-100782
Additional information on 2-Fluoro-4-(trifluoromethyl)aniline
Introduction to 2-Fluoro-4-(trifluoromethyl)aniline (CAS No. 69403-12-9)
2-Fluoro-4-(trifluoromethyl)aniline (CAS No. 69403-12-9) is a versatile organic compound that has garnered significant attention in the fields of pharmaceuticals, agrochemicals, and materials science. This compound is characterized by its unique combination of a fluorine atom and a trifluoromethyl group attached to an aniline backbone, which imparts it with distinct chemical and physical properties. These properties make it an essential building block in the synthesis of various advanced materials and pharmaceutical intermediates.
The molecular structure of 2-Fluoro-4-(trifluoromethyl)aniline consists of a benzene ring with a fluorine atom at the 2-position and a trifluoromethyl group at the 4-position, along with an amino group (-NH2) attached to the benzene ring. The presence of these functional groups significantly influences the compound's reactivity and stability, making it highly suitable for a wide range of synthetic transformations.
In the pharmaceutical industry, 2-Fluoro-4-(trifluoromethyl)aniline is often used as an intermediate in the synthesis of drugs with potent biological activities. For instance, it has been utilized in the development of selective serotonin reuptake inhibitors (SSRIs), which are widely prescribed for treating depression and anxiety disorders. Recent studies have also explored its potential in the synthesis of novel antiviral agents, particularly those targeting viral proteases involved in the replication of RNA viruses such as influenza and SARS-CoV-2.
The unique electronic properties of 2-Fluoro-4-(trifluoromethyl)aniline make it an attractive candidate for use in materials science applications. Its ability to form stable complexes with various metal ions has led to its use in the development of luminescent materials and sensors. For example, researchers have synthesized coordination polymers using this compound as a ligand, which exhibit enhanced photoluminescence properties and can be used for detecting specific analytes in environmental monitoring.
In the agrochemical sector, 2-Fluoro-4-(trifluoromethyl)aniline has found applications in the synthesis of herbicides and fungicides. The introduction of fluorine atoms into these compounds can improve their selectivity and efficacy, reducing the environmental impact while maintaining high agricultural productivity. Recent advancements in green chemistry have also focused on developing more sustainable methods for synthesizing this compound, aiming to minimize waste and energy consumption during production processes.
The synthesis of 2-Fluoro-4-(trifluoromethyl)aniline typically involves multi-step reactions starting from readily available starting materials. One common approach is to use 4-trifluoromethylaniline as a starting point, followed by selective fluorination at the 2-position. Advances in catalytic methods have significantly improved the yield and purity of this compound, making it more accessible for industrial applications.
Safety considerations are paramount when handling 2-Fluoro-4-(trifluoromethyl)aniline. While it is not classified as a hazardous material under current regulations, proper safety protocols should be followed to ensure safe handling and storage. This includes using appropriate personal protective equipment (PPE) such as gloves and goggles, working in well-ventilated areas, and storing the compound away from incompatible substances.
In conclusion, 2-Fluoro-4-(trifluoromethyl)aniline (CAS No. 69403-12-9) is a valuable compound with diverse applications across multiple industries. Its unique chemical structure and properties make it an essential component in the development of advanced materials, pharmaceuticals, and agrochemicals. Ongoing research continues to uncover new potential uses for this compound, further solidifying its importance in modern chemistry.
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