4-(Trifluoromethoxy)aniline
4-(Trifluoromethoxy)aniline structure
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Common Name | 4-(Trifluoromethoxy)aniline | ||
|---|---|---|---|---|
| CAS Number | 461-82-5 | Molecular Weight | 177.13 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 192.4±0.0 °C at 760 mmHg | |
| Molecular Formula | C7H6F3NO | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 80.6±0.0 °C | |
| Symbol |
GHS05, GHS06, GHS08 |
Signal Word | Danger | |
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The metabolism of 4-trifluoromethoxyaniline and [13C]-4-trifluoromethoxyacetanilide in the rat: detection and identification of metabolites excreted in the urine by NMR and HPLC-NMR.
J. Pharm. Biomed. Anal. 28(5) , 875-85, (2002) A combination of 19F, 1H NMR and HPLC-NMR spectroscopic approaches have been used to quantify and identify the urinary-excreted metabolites of 4-trifluoromethoxyaniline (4-TFMeA) and its [13C]-labelled acetanilide following i.p. administration at 50 mg/kg to ... |
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Synthesis of liquid-crystalline poly (meth) acrylates with 4-trifluoromethoxy-azobenzene mesogenic side-groups. Prescher D, et al.
J. Fluor. Chem. 74(2) , 185-89, (1995)
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Microwave-assisted multistep synthesis of functionalized 4-arylquinolin-2 (1 H)-ones using palladium-catalyzed cross-coupling chemistry. Glasnov TN, et al.
J. Org. Chem. 70(10) , 3865-70, (2005)
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Addition of Me3SiCN to trifluoromethyl derivates of N-(pyridylmethylidene) anilines catalyzed by Lewis acids. Iovel I, et al.
Appl. Organomet. Chem. 15(9) , 733-43, (2001)
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