No renderable structure data available
CCOC(=O)CCC(=O)OChemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | 4-ethoxy-4-oxobutanoic acid |
|---|---|
| IUPAC Name | — |
| CAS Number | 1070-34-4 |
| Database ID | 70610 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
4-ethoxy-4-oxobutanoic acid (CAS 1070-34-4) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
Potential Applications
For professional research and industrial use only
Database ID 70610
Safety Notice
For professional research and industrial use only. Review the supplier safety data sheet before handling.
Synthesis data
12 reactions · 12 references
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-2f94428f24184c4ca34f7e9b1243cdabConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-46a11445c3344f809803132b7eaa9c50Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-05a268e846604ae9b51c385fed52bf30Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-565f2e5cdab7400da3d2c1b9b1a9984bConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-db33e5b0df0e4b92a64669164b79c837Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-2f94428f24184c4ca34f7e9b1243cdabConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-46a11445c3344f809803132b7eaa9c50Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-46a11445c3344f809803132b7eaa9c50Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: 250 mg of 3-amino-7-(cyclohexylamino)-1-cyclopentyl-6-fluoroquinoline-4(1H)-one and 127 mg of 4-ethoxy-4-oxobutanoic acid were dissolved in 20 ml of DMF, and 170 mg of N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride and 160 mg of 1-hydroxybenzotriazole were added, followed by overnight stirring at room temperature. By adding water to the reaction mixture and collecting the insoluble materials by filtration, 220 mg of ethyl 4-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}-4-oxobutanoate was obtained. collecting the insoluble materials by filtration
Source ID: ord-4093c6738de74199bf76f820fbc728fbConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: 250 mg of 3-amino-7-(cyclohexylamino)-1-cyclopentyl-6-fluoroquinoline-4(1H)-one and 127 mg of 4-ethoxy-4-oxobutanoic acid were dissolved in 20 ml of DMF, and 170 mg of N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride and 160 mg of 1-hydroxybenzotriazole were added, followed by overnight stirring at room temperature. By adding water to the reaction mixture and collecting the insoluble materials by filtration, 220 mg of ethyl 4-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}-4-oxobutanoate was obtained. collecting the insoluble materials by filtration
Source ID: ord-aa6639433f2f4555a4b940ef4fcbad39Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: 250 mg of 3-amino-7-(cyclohexylamino)-1-cyclopentyl-6-fluoroquinoline-4(1H)-one and 127 mg of 4-ethoxy-4-oxobutanoic acid were dissolved in 20 ml of DMF, and 170 mg of N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride and 160 mg of 1-hydroxybenzotriazole were added, followed by overnight stirring at room temperature. By adding water to the reaction mixture and collecting the insoluble materials by filtration, 220 mg of ethyl 4-{[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]amino}-4-oxobutanoate was obtained. collecting the insoluble materials by filtration
Source ID: ord-aa6639433f2f4555a4b940ef4fcbad39Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-05a268e846604ae9b51c385fed52bf30PubChem References
These sources are listed in the compound's public database record.
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