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CAS 54716-02-8

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Ethyl (2E)-3-(1-pyrrolidinyl)-2-butenoate

Description:
Ethyl (2E)-3-(1-pyrrolidinyl)-2-butenoate, with the CAS number 54716-02-8, is an organic compound characterized by its ester functional group and a pyrrolidine ring. This compound features a butenoate backbone, which contributes to its reactivity and potential applications in organic synthesis. The presence of the pyrrolidinyl group enhances its biological activity, making it of interest in medicinal chemistry. Ethyl (2E)-3-(1-pyrrolidinyl)-2-butenoate is typically a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents, which facilitates its use in various chemical reactions. The compound may exhibit properties such as moderate volatility and stability under standard conditions, but it should be handled with care due to potential reactivity. Its unique structure allows for various applications, including use as an intermediate in the synthesis of pharmaceuticals or agrochemicals. As with many organic compounds, safety data sheets should be consulted for handling and storage guidelines to ensure safe usage in laboratory or industrial settings.
Formula:C10H17NO2
InChI:InChI=1S/C10H17NO2/c1-3-13-10(12)8-9(2)11-6-4-5-7-11/h8H,3-7H2,1-2H3/b9-8+
InChI key:InChIKey=MSOQKPXSIHLODG-CMDGGOBGSA-N
SMILES:C(=C\C(OCC)=O)(\C)/N1CCCC1
Synonyms:
  • (E)-Ethyl 3-(pyrrolidin-1-yl)but-2-enoate
  • 2-Butenoic acid, 3-(1-pyrrolidinyl)-, ethyl ester, (2E)-
  • 2-Butenoic acid, 3-(1-pyrrolidinyl)-, ethyl ester, (E)-
  • Ethyl (2E)-3-(1-pyrrolidinyl)-2-butenoate
  • Ethyl (E)-3-(1-pyrrolidino)-2-butenoate
  • Ethyl (E)-3-(pyrrolidino)-2-butenoate
  • Ethyl acetoacetate pyrrolidinyl enamine
  • ethyl (2E)-3-(pyrrolidin-1-yl)but-2-enoate
  • ethyl (2Z)-3-(pyrrolidin-1-yl)but-2-enoate
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