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| 4-(Trifluoromethoxy)aniline Basic information |
| 4-(Trifluoromethoxy)aniline Chemical Properties |
Boiling point | 73-75 °C10 mm Hg(lit.) | density | 1.32 g/mL at 20 °C(lit.) | refractive index | n20/D 1.463(lit.) | Fp | 177 °F | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | solubility | Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly) | pka | 3.75±0.10(Predicted) | form | Liquid | color | Clear colorless to yellow | Specific Gravity | 1.310 | BRN | 2090209 | Stability: | Hygroscopic | InChI | InChI=1S/C7H6F3NO/c8-7(9,10)12-6-3-1-5(11)2-4-6/h1-4H,11H2 | InChIKey | XUJFOSLZQITUOI-UHFFFAOYSA-N | SMILES | C1(N)=CC=C(OC(F)(F)F)C=C1 | CAS DataBase Reference | 461-82-5(CAS DataBase Reference) |
| 4-(Trifluoromethoxy)aniline Usage And Synthesis |
Chemical Properties | CLEAR YELLOW LIQUID | Uses | 4-(Trifluoromethoxy)aniline was used in the synthesis of:
- side-group liquid-crystalline polymethacrylates with fluorine-containing mesogens
- derivatives of 3-(quinolin-3-yl)acrylates
- series of novel Shiff bases, via condensation with pyridinecarboxaldehydes in the presence of molecular sieves
| Uses | 4-(Trifluoromethoxy)aniline is used in the synthesis of anticancer agents and antitumor medicaments. Also, its an intermediate in the production of labelled Riluzole, a neuroprotective agent. Modulates glutamatergic transmission. A glutamate release inhibitor. An anticonvulsant. |
| 4-(Trifluoromethoxy)aniline Preparation Products And Raw materials |
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