| Weight | 186.136 g/mol |
|---|---|
| Formula | C8H5F3N2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
2-(Trifluoromethyl)benzimidazole (312-73-2)
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- Synthesis and antiparasitic activity of 2-(Trifluoromethyl)benzimidazole derivatives (Bioorganic & Medicinal Chemistry Letters, 2001)
- Synthesis and antiprotozoal activity of some 2-(trifluoromethyl)-1H-benzimidazole bioisosteres. (European Journal of Medicinal Chemistry, 2006)
- Synthesis and biological activity of 2-(trifluoromethyl)-1H-benzimidazole derivatives against some protozoa and Trichinella spiralis (European Journal of Medicinal Chemistry, 2010)
- Synthesis and biological activity of the neuronal calcium channel blocker 2-amino-1-(2,5-dimethoxyphenyl)-5-trifluoromethyl benzimidazole (NS-649) (Bioorganic & Medicinal Chemistry Letters, 1996)
- A Novel Method for Preparation of Trifluoromethyl Substituted 2,3-dihydro-1,4- diazepine and Benzimidazole (Synthetic Communications, 2000)
- Studies on 6-chloro-5-(1-naphthyloxy)-2-(trifluoromethyl)-1H-benzimidazole/2-hydroxypropyl--cyclodextrin association: Characterization, molecular modeling studies, and in vivo anthelminthic activity (Bioorganic & Medicinal Chemistry, 2011)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC1=CC=C2C(=C1)NC(=N2)C(F)(F)F
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InChIKeyMXFMPTXDHSDMTI-UHFFFAOYSA-N
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