3-Fluoro-4-methoxyaniline
Inhibitors/Agonists
3-Fluoro-4-methoxyaniline is an organic compound with the chemical formula C7H8FNO. It is a derivative of aniline, which is widely used in the production of dyes, pharmaceuticals, and other organic compounds. 3-Fluoro-4-methoxyaniline is a versatile compound that has been studied for its potential therapeutic and industrial applications.
141.14 g/mol
141.14 g/mol
Formulation:
141.14 g/mol
Source:
Usage:
3-Fluoro-4-methoxyaniline
The product is for non-human research only. Not for therapeutic or veterinary use.
Catalog Number: BT-298381
CAS Number: 366-99-4
Molecular Formula: C7H8FNO
Molecular Weight: 141.14 g/mol
Purity: ≥ 97%
Inventory: In Stock
| Size | SKU | Price | |
|---|---|---|---|
| 1g | bt-298381-1g | $295.23 | |
| 5g | bt-298381-5g | $317.23 | |
| 10g | bt-298381-10g | $634.62 | |
| 25g | bt-298381-25g | $1,476.15 | |
| 100g | bt-298381-100g | $5,897.23 | |
| 500g | bt-298381-500g | $28,364.15 |
| CAS Number | 366-99-4 |
|---|---|
| Product Name | 3-Fluoro-4-methoxyaniline |
| Molecular Formula | C7H8FNO |
| Molecular Weight | 141.14 g/mol |
| InChI | InChI=1S/C7H8FNO/c1-10-7-3-2-5(9)4-6(7)8/h2-4H,9H2,1H3 |
| InChI Key | LJWAPDSCYTZUJU-UHFFFAOYSA-N |
| IUPAC Name | 3-fluoro-4-methoxyaniline |
| Canonical SMILES | COC1=C(C=C(C=C1)N)F |
| Description | 3-Fluoro-4-methoxyaniline is an organic compound with the chemical formula C7H8FNO. It is a derivative of aniline, which is widely used in the production of dyes, pharmaceuticals, and other organic compounds. 3-Fluoro-4-methoxyaniline is a versatile compound that has been studied for its potential therapeutic and industrial applications. |
| Method of Synthesis or Extraction | There are several methods for synthesizing 3-Fluoro-4-methoxyaniline, including the reaction of 3-fluoroaniline with methoxybenzene in the presence of a catalyst, the reaction of 3-fluoroaniline with methanol in the presence of a dehydrating agent, and the reaction of 3-fluoroaniline with dimethyl sulfate followed by hydrolysis. The efficiency and yield of each method vary depending on the reaction conditions and the purity of the starting materials. The reaction of 3-fluoroaniline with methoxybenzene in the presence of a catalyst has been reported to yield 70-80% of the desired product. However, this method requires a high temperature and pressure, which can be hazardous and energy-intensive. The reaction of 3-fluoroaniline with methanol in the presence of a dehydrating agent has been reported to yield 60-70% of the desired product. This method is relatively simple and safe, but it requires a longer reaction time and may produce impurities. The reaction of 3-fluoroaniline with dimethyl sulfate followed by hydrolysis has been reported to yield 50-60% of the desired product. This method is efficient and produces a high purity product, but it requires the use of a toxic and carcinogenic reagent. |
| Chemical Structure and Biological Activity | The chemical structure of 3-Fluoro-4-methoxyaniline consists of a fluorine atom, a methoxy group, and an amino group attached to a benzene ring. The presence of the fluorine atom and the methoxy group can affect the biological activity of the compound. 3-Fluoro-4-methoxyaniline has been studied for its potential as a drug candidate for the treatment of cancer, inflammation, and other diseases. The mechanism of action and biological targets of 3-Fluoro-4-methoxyaniline are not fully understood, but it is believed to act by inhibiting specific enzymes or signaling pathways in cells. The bioactivity and potency of 3-Fluoro-4-methoxyaniline vary depending on the specific biological target and the concentration of the compound. |
| Biological Effects | The biological effects of 3-Fluoro-4-methoxyaniline on cell function and signal transduction have been studied in vitro and in vivo. In vitro studies have shown that 3-Fluoro-4-methoxyaniline can inhibit the growth and proliferation of cancer cells, reduce inflammation, and modulate the immune response. In vivo studies have shown that 3-Fluoro-4-methoxyaniline can reduce tumor growth and improve survival in animal models of cancer. However, the potential therapeutic and toxic effects of 3-Fluoro-4-methoxyaniline in humans are not yet known and require further investigation. |
| Applications | 3-Fluoro-4-methoxyaniline has potential applications in medical research, environmental research, and industrial research. In medical research, 3-Fluoro-4-methoxyaniline may have a role in drug development as a potential therapeutic agent for cancer, inflammation, and other diseases. Clinical trials and findings are needed to determine the safety and efficacy of 3-Fluoro-4-methoxyaniline in humans. In environmental research, 3-Fluoro-4-methoxyaniline may have effects on ecosystems and may be useful in pollution management and sustainability efforts. In industrial research, 3-Fluoro-4-methoxyaniline may be used in manufacturing processes to improve product quality and efficiency. Health and safety considerations must be taken into account when using 3-Fluoro-4-methoxyaniline in industrial settings. |
| Future Perspectives and Challenges | The current limitations in the use and study of 3-Fluoro-4-methoxyaniline include the lack of understanding of its mechanism of action and biological targets, the potential toxicity and side effects, and the need for further research to determine its safety and efficacy in humans. Possible solutions and improvements include the development of more efficient and environmentally friendly methods of synthesis or extraction, the identification of specific biological targets and pathways, and the optimization of the compound's pharmacokinetic and pharmacodynamic properties. Future trends and prospects in the application of 3-Fluoro-4-methoxyaniline in scientific research include the development of personalized medicine and the use of combination therapies to improve treatment outcomes. |
| Pictograms | Irritant |
| SMILES | COC1=C(C=C(C=C1)N)F |
| Synonyms | 3-Fluoro-4-methoxybenzenamine; (3-Fluoro-4-methoxyphenyl)amine; 3-Fluoro-p-anisidine; 3-Fluoroanisidine; 4-Amino-2-fluoroanisole; [3-Fluoro-4-(methyloxy)phenyl]amine; |
| Reference | Gao et al. Rapid heteroatom-transfer to arylmetals utilizing multifunctional reagent scaffolds. Nature Chemistry, doi: 10.1038/nchem.2672, published online 28 November 2016 |
| PubChem Compound | 3-Fluoro-4-methoxyaniline |
| Last Modified | May 29 2023 |