CAS 611-10-9
:Ethyl 2-oxocyclopentanecarboxylate
Description:
Ethyl 2-oxocyclopentanecarboxylate, with the CAS number 611-10-9, is an organic compound characterized by its ester functional group and a cyclopentanecarboxylic acid derivative structure. It typically appears as a colorless to pale yellow liquid with a pleasant, fruity odor. This compound is known for its moderate volatility and solubility in organic solvents, making it useful in various chemical applications. Ethyl 2-oxocyclopentanecarboxylate features a carbonyl group adjacent to a cyclopentane ring, which contributes to its reactivity, particularly in nucleophilic addition reactions. It can serve as an intermediate in organic synthesis, particularly in the preparation of more complex molecules. Additionally, it may exhibit mild toxicity, necessitating proper handling and safety precautions during use. Overall, its unique structure and properties make it a valuable compound in synthetic organic chemistry and related fields.
Formula:C8H12O3
InChI:InChI=1S/C8H12O3/c1-2-11-8(10)6-4-3-5-7(6)9/h6H,2-5H2,1H3
InChI key:InChIKey=JHZPNBKZPAWCJD-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C1C(=O)CCC1
Synonyms:- (.+-.)-2-Oxocyclopentanecarboxylic acid ethyl ester
- 1-Oxocyclopentane-2-carboxylic acid ethyl ester
- 2-(Ethoxycarbonyl)-1-cyclopentanone
- 2-(Ethoxycarbonyl)cyclopentanone
- 2-Carbethoxy-1-cyclopentanone
- 2-Carbethoxycyclopentanone
- 2-Carboethoxycyclopentanone
- 2-Cyclopentanonecarboxylic acid ethyl ester
- 2-Oxociclopentanocarboxilato De Etilo
- 2-Oxocyclopentane-1-carboxylic acid ethyl ester
- 2-Oxocyclopentanecarboxylate D'Ethyle
- Ethyl (.+-.)-2-oxocyclopentanecarboxylate
- Ethyl 1-oxocyclopentane-2-carboxylate
- Ethyl 2-cyclopentanone-1-carboxylate
- Ethyl 2-cyclopentanonecarboxylate
- Ethyl 2-oxo-1-cyclopentanecarboxylate
- Ethyl 2-oxocyclopentanoate
- Ethyl 2-oxocyclopentylcarboxylate
- Ethyl-2-oxocyclopentancarboxylat
- Nsc 22055
- Nsc 5658
- α-(Carboethoxy)cyclopentanone
- See more synonyms
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Found 7 products.
Ethyl 2-Oxocyclopentanecarboxylate
CAS:Formula:C8H12O3Purity:>97.0%(GC)Color and Shape:Colorless to Light yellow clear liquidMolecular weight:156.18Ethyl 2-oxocyclopentanecarboxylate, 97+%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C8H12O3Purity:97+%Color and Shape:Liquid, Clear colorless to pale yellowMolecular weight:156.18Ethyl 2-Oxocyclopentanecarboxylate
CAS:Formula:C8H12O3Purity:94%Color and Shape:LiquidMolecular weight:156.17912-Carbethoxycyclopentanone
CAS:Formula:C8H12O3Purity:≥ 96.0%Color and Shape:Clear, colourless to light-yellow liquidMolecular weight:156.18Ethyl 2-oxocyclopentanecarboxylate
CAS:Formula:C8H12O3Purity:94%Color and Shape:ClearMolecular weight:156.181Ethyl 2-oxocyclopentanecarboxylate
CAS:<p>Ethyl 2-oxocyclopentanecarboxylate</p>Purity:97%Color and Shape:Pale Yellow LiquidMolecular weight:156.18g/molEthyl cyclopentanone-2-carboxylate
CAS:<p>Ethyl cyclopentanone-2-carboxylate (ECPC) is a chemical compound that can be synthesized from picolinic acid, β-amino acid, and methyl ketones. It is a bifunctional molecule that has been shown to have the ability to activate methylene groups. ECPC has been used in the synthesis of β-amino esters and ethyl esters. This compound can also react with hydrogen fluoride and trifluoroacetic acid to form ethyl cyclopentanone-2-carboxylate trifluoroacetate (ECPCT). ECPC has been found to undergo an aldol cyclization reaction when exposed to hydrogen ions in the presence of a base. The activation energies for this reaction are 19.6 kJ/mol for the first step and 23.5 kJ/mol for the second step.</p>Formula:C8H12O3Purity:Min. 95 Area-%Color and Shape:Colorless Clear LiquidMolecular weight:156.18 g/mol






