208744
(2-Fluorophenyl)acetone
99%
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About This Item
Linear Formula:
FC6H4CH2COCH3
CAS Number:
Molecular Weight:
152.17
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
220-627-5
MDL number:
Assay:
99%
Form:
liquid
InChI key
BANVZEUCJHUPOI-UHFFFAOYSA-N
InChI
1S/C9H9FO/c1-7(11)6-8-4-2-3-5-9(8)10/h2-5H,6H2,1H3
SMILES string
CC(=O)Cc1ccccc1F
assay
99%
form
liquid
refractive index
n20/D 1.4989 (lit.)
bp
47 °C/0.05 mmHg (lit.)
density
1.077 g/mL at 25 °C (lit.)
Application
(2-Fluorophenyl)acetone was used in the synthesis of 6-methyluracils.
General description
(2-Fluorophenyl)acetone on reaction with chlorosulfonyl isocyanate yields 5-(2-fluorophenyl)-6-methyl-1,3-oxazine-2,4-(3H)-dione.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
185.0 °F - closed cup
flash_point_c
85 °C - closed cup
Regulatory Information
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Jennifer A Weiß et al.
Science & justice : journal of the Forensic Science Society, 57(1), 6-12 (2017-01-09)
Amphetamine and its derivatives gained high popularity on the illegal drug market. In the last few years, a lot of new psychoactive compounds structurally related to amphetamine, such as 4-fluoroamphetamine and 4-fluoromethamphetamine swamped the drug market. They were designed to
Martin W Rowbottom et al.
Bioorganic & medicinal chemistry letters, 14(9), 2269-2274 (2004-04-15)
The synthesis of a series of (R)-1-alkyl-3-[2-(2-amino)phenethyl]-5-(2-fluorophenyl)-6-methyluracils is discussed. SAR around N-1 of the uracil was explored, which led to the discovery that an electron-deficient 2,6-disubstituted benzyl group is required for optimal receptor binding. The best compound from the series
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