Ethyl 3-(3-furyl)-3-oxopropanoate

Names

[ Name ]:
Ethyl 3-(3-furyl)-3-oxopropanoate

[Synonym ]:
ETHYL 3-OXO-3-(FURAN-3-YL)PROPANOATE
Ethyl beta-oxo-3-furanpropionate
3-Furanpropanoic acid, β-oxo-, ethyl ester
Ethyl 3-(3-furyl)-3-oxopropanoate
MFCD00011566
ethyl 3-(furan-3-yl)-3-oxopropanoate

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
268.0±0.0 °C at 760 mmHg

[ Molecular Formula ]:
C₉H₁₀O₄

[ Molecular Weight ]:
182.173

[ Flash Point ]:
99.3±20.4 °C

[ Exact Mass ]:
182.057907

[ PSA ]:
56.51000

[ LogP ]:
1.02

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.476

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2932190090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2932190090

[ Summary ]:
2932190090 other compounds containing an unfused furan ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

Articles

Detection of glutathione conjugates derived from 4-ipomeanol metabolism in bile of rats by liquid chromatography-tandem mass spectrometry.

Drug Metab. Dispos. 32(12) , 1345-50, (2004)

Earlier studies postulated that bioactivation of 4-ipomeanol by cytochrome P450 enzymes may occur through oxidation of its furan ring, following a mechanism similar to the bioactivation of other furan...