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| IUPAC Name: | 2,2,2-trifluoro-1-piperidin-1-ylethanone |
| Description: | 1-Trifluoroacetyl piperidine (CAS# 340-07-8) is a reactant for synthesis of: photoreactive probes that differentiate the binding sites of noncompetitive GABA receptor antagonists; photoactive a-mannosides and mannosyl peptides; photoaffinity labeled fusidic acid analogues; hydroxyamides as anticonvulsants. |
| Molecular Weight: | 181.16 |
| Molecular Formula: | C7H10F3NO |
| Canonical SMILES: | C1CCN(CC1)C(=O)C(F)(F)F |
| InChI: | InChI=1S/C7H10F3NO/c8-7(9,10)6(12)11-4-2-1-3-5-11/h1-5H2 |
| InChI Key: | BCJUMGSHTLYECD-UHFFFAOYSA-N |
| Boiling Point: | 247.5 ℃ at 760 mmHg |
| Density: | 1.226 g/cm3 |
| Appearance: | Light yellow oil |
| MDL: | MFCD00466213 |
| LogP: | 1.49910 |
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Piperidines
Ethyl 1-(1-methylpyrazolo[3,4-d]pyrimidin-4-yl)piperidine-4-carboxylate
Ethyl 1-(1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)piperidine-4-carboxylate
Ethyl 1-(4-(1,5-dimethyl-1H-pyrazol-4-yl)-6-(trifluoromethyl)pyrimidin-2-yl)piperidine-3-carboxylate
Ethyl 1-(4-(3-methoxyphenyl)-6-(trifluoromethyl)pyrimidin-2-yl)piperidine-3-carboxylate
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