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CAS 7149-65-7

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H-Pyr-OEt

Description:
H-Pyr-OEt, also known as 2-(2-ethoxy-2-oxoethyl)-1H-pyrrole, is a chemical compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing nitrogen. This compound typically exhibits properties associated with both pyrrole derivatives and ethoxy groups, contributing to its reactivity and potential applications in organic synthesis. H-Pyr-OEt may participate in various chemical reactions, including nucleophilic substitutions and cycloadditions, due to the presence of functional groups that can act as electrophiles or nucleophiles. Its solubility is generally influenced by the ethoxy group, which can enhance its compatibility with organic solvents. The compound's unique structure may also impart specific biological activities, making it of interest in medicinal chemistry. As with many organic compounds, safety data should be consulted to understand its handling and potential hazards. Overall, H-Pyr-OEt represents a versatile building block in synthetic organic chemistry, with potential applications in pharmaceuticals and materials science.
Formula:C7H11NO3
InChI:InChI=1/C7H11NO3/c1-2-11-7(10)5-3-4-6(9)8-5/h5H,2-4H2,1H3,(H,8,9)
InChI key:InChIKey=QYJOOVQLTTVTJY-YFKPBYRVSA-N
SMILES:C(OCC)(=O)[C@@H]1CCC(=O)N1
Synonyms:
  • (2S)-5-Oxopyrrolidine-2-carboxylic acid ethyl ester
  • (S)-(+)-Ethyl 2-pyrrolidone-5-carboxylate
  • (S)-Ethyl 5-oxopyrrolidine-2-carboxylate
  • <span class="text-smallcaps">L</span>-2-Ethoxycarbonyl-5-pyrrolidone
  • <span class="text-smallcaps">L</span>-Proline, 5-oxo-, ethyl ester
  • <span class="text-smallcaps">L</span>-Pyroglutamic acid ethyl ester
  • Ethyl (2S)-5-oxopyrrolidine-2-carboxylate
  • Ethyl (S)-pyroglutamate
  • Ethyl 5-oxo-<span class="text-smallcaps">L</span>-prolinate
  • Ethyl <span class="text-smallcaps">L</span>-2-oxo-5-pyrrolidinecarboxylate
  • See more synonyms
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