AE20198
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 95% | in stock | $90.00 | $63.00 | - + | |
1g | 95% | in stock | $135.00 | $95.00 | - + | |
5g | 95% | in stock | $328.00 | $230.00 | - + | |
10g | 95% | in stock | $546.00 | $382.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AE20198 |
Chemical Name: | 4-Phenoxy-2-(trifluoromethyl)aniline |
CAS Number: | 106877-21-8 |
Molecular Formula: | C13H10F3NO |
Molecular Weight: | 253.2198 |
MDL Number: | MFCD08688475 |
SMILES: | Nc1ccc(cc1C(F)(F)F)Oc1ccccc1 |
4-phenoxy-2-(trifluoromethyl)aniline is a versatile compound that finds extensive application in chemical synthesis. Its unique structure allows for a variety of reactions and transformations, making it a valuable building block in organic chemistry.One key application of this compound is its role as a nucleophilic aromatic substitution (S<sub>N</sub>Ar) reagent. The phenoxide group provides a nucleophilic site for attacking electrophilic aromatic systems, while the trifluoromethyl group enhances the reactivity and stability of the intermediate species. This reaction pathway enables the introduction of the phenoxy-trifluoromethyl moiety into different organic molecules, leading to the synthesis of complex structures with diverse properties.In addition, 4-phenoxy-2-(trifluoromethyl)aniline can serve as a precursor for the synthesis of various biologically active compounds, agrochemicals, and materials. The presence of both electron-donating and electron-withdrawing substituents in its structure offers opportunities for fine-tuning the reactivity and selectivity in different synthetic pathways.Overall, the strategic incorporation of 4-phenoxy-2-(trifluoromethyl)aniline in chemical synthesis enables the construction of novel molecules with tailored functionalities and promising applications across various fields of chemistry.