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mp
71-73 °C (lit.)
SMILES string
CCOC(=O)CC(=O)c1ccc(cc1)[N+]([O-])=O
InChI
1S/C11H11NO5/c1-2-17-11(14)7-10(13)8-3-5-9(6-4-8)12(15)16/h3-6H,2,7H2,1H3
InChI key
NGRXSVFCLHVGKU-UHFFFAOYSA-N
Application
- Synthesis of β-1,3-dicarbonyl aldehydes via oxidation
- Knoevenagel condensation using a lysine catalyst
- Cycloisomerization fo rthe synthesis of trisubstituted furans
- Fluorination by HF and iodosylbenzene
- Intramolecular Michael addition reactions for synthesis of benzylbutyrolactones
- Synthesis of diols via reduction of aromatic and aliphatic ketos esters
- Cross-coupling reactions for stereoselective synthesis of unsymmetrical 1,4-enediones
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Articles
Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.
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