Ethyl 3-oxoglutarate
Names
[ CAS No. ]:
105-50-0
[ Name ]:
Ethyl 3-oxoglutarate
[Synonym ]:
Diethyl acetone-1,3-dicarboxylate or 3-Oxo-pentanedioic acid, diethy ester
ETHYL ACETONEDICARBOXYLATE
Glutaric acid, 3-oxo-, diethyl ester
Ethyl 3-oxoglutarate
diethylacetone dicarboxylate
Pentanedioic acid, 3-oxo-, diethyl ester
DIETHYL 3-KETOGLUTARATE
DIETHYL 3-OXOGLUTARATE
Diethyl-3-oxopentaediote
Diethyl β-oxoglutarate
1,3-Acetonedicarboxylic Acid Diethyl Ester
3-Oxopentanedioic acid diethyl ester
Diethyl 3-oxopentanedioate
Glutaric acid, 3-oxo-, diethyl ester (8CI)
EINECS 203-302-2
3-oxoglutaric acid diethyl ester
Diethyl-3-oxo-pentan
Diethyl Acetone-1,3-Dicarboxylate
MFCD00009200
Biological Activity
[Description]:
[Related Catalog]:
[In Vitro]
Chemical & Physical Properties
[ Density]:
1.1±0.1 g/cm3
[ Boiling Point ]:
250.0±0.0 °C at 760 mmHg
[ Molecular Formula ]:
C9H14O5
[ Molecular Weight ]:
202.21
[ Flash Point ]:
86.1±0.0 °C
[ Exact Mass ]:
202.084122
[ PSA ]:
69.67000
[ LogP ]:
2.08
[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C
[ Index of Refraction ]:
1.435
[ Storage condition ]:
2-8°C
[ Water Solubility ]:
10 g/L (20 ºC)
MSDS
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
[ Hazard Codes ]:
F: Flammable;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S23-S24/25
[ RIDADR ]:
UN 2810
[ WGK Germany ]:
3
[ HS Code ]:
2942000000
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
Anticancer Drug Des. 15(2) , 99-108, (2000)
A series of novel pyrido[4,3,2-de]quinoline and isoquinolino[6,5,4,3-cde] quinoline compounds was synthesized and evaluated for cytotoxicity in the National Cancer Institute developmental therapeutics...
A synthesis of the pyrazomycins.J. Org. Chem. 41(2) , 287-90, (1976)
A practical synthesis of (±)-thienamycin. Melillo DG, et al.
Tetrahedron Lett. 21(29) , 2783-86, (1980)