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| | 4-Aminobenzotrifluoride Basic information |
| | 4-Aminobenzotrifluoride Chemical Properties |
| Melting point | 3-8 °C | | Boiling point | 83 °C12 mm Hg(lit.) | | density | 1.283 g/mL at 25 °C(lit.) | | refractive index | n20/D 1.483(lit.) | | Fp | 188 °F | | storage temp. | Keep in dark place,Inert atmosphere,2-8°C | | solubility | DMSO (Slightly), Methanol (Slightly) | | form | Liquid | | pka | 2.45(at 25℃) | | color | Clear colorless to yellow | | Specific Gravity | 1.283 | | Water Solubility | <0.1 g/100 mL | | Sensitive | Air Sensitive | | BRN | 1564853 | | InChIKey | ODGIMMLDVSWADK-UHFFFAOYSA-N | | LogP | 1.95 at 20℃ | | CAS DataBase Reference | 455-14-1(CAS DataBase Reference) | | NIST Chemistry Reference | Benzenamine, 4-(trifluoromethyl)-(455-14-1) | | EPA Substance Registry System | 4-(Trifluoromethyl)aniline (455-14-1) |
| | 4-Aminobenzotrifluoride Usage And Synthesis |
| Chemical Properties | clear colorless to yellow liquid | | Uses | 4-(Trifluoromethyl)aniline was used in the synthesis of 4-(trialkylmethyl)anilines. It was also used as a synthetic building block. | | Uses | 4-Substituted aniline derivatives exert special hematotoxicity on the red blood cells and induce leukocytosis. | | Definition | ChEBI: A substituted aniline that is a benzene ring substituted with an amino group at position 1 and a trifluoromethyl group at position 4. | | Synthesis Reference(s) | The Journal of Organic Chemistry, 54, p. 2873, 1989 DOI: 10.1021/jo00273a020 | | General Description | Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards. |
| | 4-Aminobenzotrifluoride Preparation Products And Raw materials |
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