263362
3′,5′-双(三氟甲基)苯乙酮
98%
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关于此项目
线性分子式:
(CF3)2C6H3COCH3
化学文摘社编号:
分子量:
256.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
250-023-7
MDL number:
Assay:
98%
Form:
liquid
InChI key
MCYCSIKSZLARBD-UHFFFAOYSA-N
InChI
1S/C10H6F6O/c1-5(17)6-2-7(9(11,12)13)4-8(3-6)10(14,15)16/h2-4H,1H3
SMILES string
CC(=O)c1cc(cc(c1)C(F)(F)F)C(F)(F)F
assay
98%
form
liquid
refractive index
n20/D 1.4221 (lit.)
density
1.422 g/mL at 25 °C (lit.)
functional group
fluoro, ketone
Quality Level
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
179.6 °F - closed cup
flash_point_c
82 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
S Kneubühler et al.
Journal of medicinal chemistry, 38(19), 3874-3883 (1995-09-15)
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 values) to high (submicromolar IC50 values)
Rhodium-catalyzed heterogeneous enantioselective hydrogenation of 3, 5-di-(trifluoromethyl)-acetophenone.
Hess R, et al.
J. Mol. Catal. A: Chem., 212(1), 205-209 (2004)
Pu Wang et al.
Applied microbiology and biotechnology, 90(6), 1897-1904 (2011-05-27)
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)phenyl] ethanol with high enantiometric excess (ee) value. Based on its morphological
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