| Weight | 189.136 g/mol |
|---|---|
| Formula | C8H6F3NO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
3-(Trifluoromethyl)benzamide (1801-10-1)
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- Discovery of 3-[2-(imidazo[1,2-b]pyridazin-3-yl)ethynyl]-4-methyl-N-{4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}benzamide (AP24534), a potent, orally active pan-inhibitor of breakpoint cluster region-abelson (BCR-ABL) kinase including the T315I gatekeeper mutant. (Journal of Medicinal Chemistry, 2010)
- Effects of AF3442 [N-(9-ethyl-9H-carbazol-3-yl)-2-(trifluoromethyl)benzamide], a novel inhibitor of human microsomal prostaglandin E synthase-1, on prostanoid biosynthesis in human monocytes in vitro. (Biochemical Pharmacology, 2010)
- Catalytic Activity of epi-Quinine-Derived 3,5-Bis(trifluoromethyl)benzamide in Asymmetric Nitro-Michael Reaction of Furanones (Organic Letters, 2015)
- 2-Chloro-N-[(S)-phenyl [(2S)-piperidin-2-yl] methyl]-3-trifluoromethyl benzamide, monohydrochloride, an inhibitor of the glycine transporter type 1, increases evoked-dopamine release in the rat nucleus accumbens in vivo via an enhanced glutamatergic neurotransmission. (Neuroscience, 2006)
- Stereoselective preparation of N-[(R, R)-(E)-1-(3,4-dichlorobenzyl)-3-(2-oxoazepan-3-yl) carbamoyl] allyl-N-methyl-3,5-bis (trifluoromethyl) benzamide, a potent and orally active dual neurokinin NK (1)/NK (2) receptor antagonist (Journal of Medicinal Chemistry, 2003)
- N-[(R,R)-(E)-1-(4-chloro-benzyl)-3-(2-oxo-azepan-3-ylcarbamoyl)-allyl]-N-methyl-3,5-bis-trifluoromethyl-benzamide: an orally active neurokinin NK1/NK2 antagonist. (Bioorganic & Medicinal Chemistry Letters, 2000)
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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)C(=O)N
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InChIKeyXBGXGCOLWCMVOI-UHFFFAOYSA-N
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