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CAS 887411-85-0

:

ethyl 3-oxo-3-(tetrahydrofuran-2-yl)propanoate

Description:
Ethyl 3-oxo-3-(tetrahydrofuran-2-yl)propanoate is an organic compound characterized by its ester functional group and a cyclic ether moiety. It features a propanoate backbone with a keto group at the central carbon, which contributes to its reactivity and potential applications in organic synthesis. The presence of the tetrahydrofuran ring enhances its solubility in organic solvents and may influence its chemical behavior, such as reactivity in nucleophilic addition reactions. This compound is typically a colorless to pale yellow liquid, with a pleasant odor, and is likely to be stable under standard conditions. Its molecular structure suggests potential uses in pharmaceuticals, agrochemicals, or as an intermediate in the synthesis of more complex molecules. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken due to potential toxicity or reactivity. Overall, ethyl 3-oxo-3-(tetrahydrofuran-2-yl)propanoate represents a versatile building block in synthetic organic chemistry.
Formula:C9H14O4
InChI:InChI=1/C9H14O4/c1-2-12-9(11)6-7(10)8-4-3-5-13-8/h8H,2-6H2,1H3
SMILES:CCOC(=O)CC(=O)C1CCCO1
Synonyms:
  • ETHYL 3-OXO-3-(TETRAHYDROFURAN-2-YL)PROPANOATE
  • Ethyl 3-Oxo-3-(2-tetrahydrofuryl)propanoate
  • ethyl 3-oxo-3-(oxolan-2-yl)propanoate
  • ETHYL 3-(TETRAHYDROFURAN-2-YL)-3-OXOPROPANOATE
  • Ethyl 3-oxo-3-(tetrahydrofuran-2-yl)
  • ETHYL-2-TETRAHYDROFURFUROYL-ACETATE
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