Substance
ID:339941
Names and Identifiers
IUPAC Traditional name
ethyl 3-(4-nitrophenyl)-3-oxopropanoate
IUPAC name
ethyl 3-(4-nitrophenyl)-3-oxopropanoate
Synonyms
4-硝基苯甲酰乙酸乙酯Ethyl 4-nitrobenzoylacetate(p-Nitrobenzoyl)acetic acid ethyl esterEthyl 3-oxo-3-(4-nitrophenyl)propanoateNSC 62134
Properties
Safety Information
Physical Property
Melting Point
71-73 °C(lit.)
Product Information
Linear Formula
O2NC6H4COCH2CO2C2H5
Molecule Details
Packaging
25 g in poly bottle
5 g in glass bottle
Application
Reactant involved in:
• Synthesis of β-1,3-dicarbonyl aldehydes via oxidation1
• Knoevenagel condensation using a lysine catalyst2
• Cycloisomerization fo rthe synthesis of trisubstituted furans3
• Fluorination by HF and iodosylbenzene4
• Intramolecular Michael addition reactions for synthesis of benzylbutyrolactones5
• Synthesis of diols via reduction of aromatic and aliphatic ketos esters6
• Cross-coupling reactions for stereoselective synthesis of unsymmetrical 1,4-enediones7
25 g in poly bottle
5 g in glass bottle
Application
Reactant involved in:
• Synthesis of β-1,3-dicarbonyl aldehydes via oxidation1
• Knoevenagel condensation using a lysine catalyst2
• Cycloisomerization fo rthe synthesis of trisubstituted furans3
• Fluorination by HF and iodosylbenzene4
• Intramolecular Michael addition reactions for synthesis of benzylbutyrolactones5
• Synthesis of diols via reduction of aromatic and aliphatic ketos esters6
• Cross-coupling reactions for stereoselective synthesis of unsymmetrical 1,4-enediones7
Molecular Spectra
No Data Available
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References
No Data Available
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