3,5-双(三氟甲基)苯乙酮
3,5-双(三氟甲基)苯乙酮结构式
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常用名 | 3,5-双(三氟甲基)苯乙酮 | 英文名 | 1-(3,5-Bis(trifluoromethyl)phenyl)ethanone |
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| CAS号 | 30071-93-3 | 分子量 | 256.145 | |
| 密度 | 1.4±0.1 g/cm3 | 沸点 | 162.7±35.0 °C at 760 mmHg | |
| 分子式 | C10H6F6O | 熔点 | N/A | |
| MSDS | 中文版 美版 | 闪点 | 82.2±0.0 °C | |
| 符号 |
GHS07 |
信号词 | Warning |
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Inhibition of monoamine oxidase-B by 5H-indeno[1,2-c]pyridazines: biological activities, quantitative structure-activity relationships (QSARs) and 3D-QSARs.
J. Med. Chem. 38 , 3874-83, (1995) A large series (66 compounds) of indeno[1,2-c]pyridazin-5-ones (IPs) were synthesized and tested on their monoamine oxidase-A (MAO-A) and MAO-B inhibitory activity. All of the tested compounds acted preferentially on MAO-B displaying weak (nonmeasurable IC50 ... |
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Asymmetric biocatalytic reduction of 3,5-bis(trifluoromethyl) acetophenone to (1R)-[3,5-bis(trifluoromethyl)phenyl] ethanol using whole cells of newly isolated Leifsonia xyli HS0904.
Appl. Microbiol. Biotechnol. 90(6) , 1897-904, (2011) A novel bacterial strain HS0904 was isolated from a soil sample using 3,5-bis(trifluoromethyl) acetophenone as the sole carbon source. This bacterial isolate can asymmetrically reduce 3,5-bis(trifluoromethyl) acetophenone to (1R)-[3,5-bis(trifluoromethyl)phen... |
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Rhodium-catalyzed heterogeneous enantioselective hydrogenation of 3, 5-di-(trifluoromethyl)-acetophenone. Hess R, et al.
J. Mol. Catal. A: Chem. 212(1) , 205-9, (2004)
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