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Merck
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文件

263362

Sigma-Aldrich

3′,5′-双(三氟甲基)苯乙酮

98%

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About This Item

线性分子式:
(CF3)2C6H3COCH3
CAS号:
30071-93-3
分子量:
256.14
EC號碼:
250-023-7
MDL號碼:
MFCD00009910
分類程式碼代碼:
12352100
PubChem物質ID:
24855965
NACRES:
NA.22

化驗

98%

形狀

liquid

折射率

n20/D 1.4221 (lit.)

密度

1.422 g/mL at 25 °C (lit.)

SMILES 字串

CC(=O)c1cc(cc(c1)C(F)(F)F)C(F)(F)F

InChI

1S/C10H6F6O/c1-5(17)6-2-7(9(11,12)13)4-8(3-6)10(14,15)16/h2-4H,1H3

InChI 密鑰

MCYCSIKSZLARBD-UHFFFAOYSA-N

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相关类别

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

179.6 °F - closed cup

閃點（°C）

82 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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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
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)

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