Ethyl 3-(4-fluorophenyl)-3-oxopropanoate

Names

[ CAS No. ]:
1999-00-4

[ Name ]:
Ethyl 3-(4-fluorophenyl)-3-oxopropanoate

[Synonym ]:
Ethyl 3-(4-fluorophenyl)-3-oxopropanoate
MFCD03093631
Benzenepropanoic acid, 4-fluoro-β-oxo-, ethyl ester
4-Fluorobenzoylacetic acid ethyl ester
3-(4-Fluorophenyl)-3-oxopropionic Acid Ethyl Ester
3-(4'-Fluorophenyl)-3-oxopropanoic acid,ethyl ester
FR DV1VO2
ethyl 3-(4-fluorophenyl)-3-oxo-propanoate
Ethyl (4-Fluorobenzoyl)acetate
Ethyl 3-(4-fluorophenyl)-3-oxopropionate
ethyl p-fluorobenzoylacetate
(4-Fluorobenzoyl)acetic Acid Ethyl Ester

Biological Activity

[Description]:

Ethyl 3-(4-fluorophenyl)-3-oxopropanoate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
280.4±15.0 °C at 760 mmHg

[ Molecular Formula ]:
C₁₁H₁₁FO₃

[ Molecular Weight ]:
210.20

[ Flash Point ]:
119.6±15.3 °C

[ Exact Mass ]:
210.069229

[ PSA ]:
43.37000

[ LogP ]:
1.93

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.495

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2918300090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2918300090

[ Summary ]:
2918300090 other carboxylic acids with aldehyde or ketone function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

Comparative Use of Solvent-free KF-Al2O3 and K2CO3 in Acetone in the Synthesis of Quinoxaline 1, 4-Dioxide Derivatives Designed as Antimalarial Drug Candidates. Lima LM, et al.

J. Heterocycl. Chem. 42(7) , 1381-85, (2005)

Related Compounds

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