| Weight | 175.153 g/mol |
|---|---|
| Formula | C8H8F3N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
3-(Trifluoromethyl)benzylamine (2740-83-2)
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- Catalytic asymmetric synthesis of -(trifluoromethyl)benzylamine via cinchonidine derived base-catalyzed biomimetic 1,3-proton shift reaction (Journal of Fluorine Chemistry, 2007)
- Thermal 1,3Proton Shift Reaction and Its Application for Operationally Convenient and Improved Synthesis of (Trifluoromethyl)benzylamine. (Journal of Fluorine Chemistry, 2007)
- Simple and Convenient Synthesis of 3,5-Bis-(trifluoromethyl)benzylamine via Biomimetic 1,3-Proton Shift Reaction. (Journal of Fluorine Chemistry, 2006)
- XRD and spectral dataset of the UV-A stable nanotubes of 3,5-bis(trifluoromethyl)benzylamine derivative of tyrosine (Data in Brief, 2017)
- Antiproliferative Activity of New Schiff Bases Derived From 3Fluoro5(trifluoromethyl) benzylamine (International journal of scientific research, 2014)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC(=C1)C(F)(F)F)CN
-
InChIKeyYKNZTUQUXUXTLE-UHFFFAOYSA-N
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Similar Compounds
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