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CAS 222555-06-8

:

ethyl (2S)-2-ethoxy-3-(4-hydroxyphenyl)propanoate

Description:
Ethyl (2S)-2-ethoxy-3-(4-hydroxyphenyl)propanoate, with the CAS number 222555-06-8, is an organic compound characterized by its ester functional group, which is derived from the reaction of an alcohol and a carboxylic acid. This compound features a chiral center, indicated by the (2S) configuration, which contributes to its stereochemical properties. The presence of the ethoxy group enhances its solubility in organic solvents, while the 4-hydroxyphenyl moiety introduces potential for hydrogen bonding and reactivity due to the hydroxyl group. This compound may exhibit biological activity, making it of interest in pharmaceutical and medicinal chemistry. Its molecular structure suggests potential applications in drug development or as a synthetic intermediate. Additionally, the compound's stability, reactivity, and interactions with other molecules can be influenced by its functional groups, making it a subject of study in various chemical contexts. Overall, ethyl (2S)-2-ethoxy-3-(4-hydroxyphenyl)propanoate represents a versatile compound with potential implications in both research and industry.
Formula:C13H18O4
InChI:InChI=1/C13H18O4/c1-3-16-12(13(15)17-4-2)9-10-5-7-11(14)8-6-10/h5-8,12,14H,3-4,9H2,1-2H3/t12-/m0/s1
SMILES:CCO[C@@H](Cc1ccc(cc1)O)C(=O)OCC
Synonyms:
  • ethyl (S)-2-ethoxy-3-(4-hydroxyphenyl)propionate
  • (S)-2-Ethoxy-3-(4-Hydroxy-Phenyl)-Propionic Acid Ethyl Ester
  • Ethyl (2S)-2-ethoxy-3-(4-hydroxyphenyl)propanoate
  • (S)-Ethyl 2-ethoxy-3-(4-hydroxyphenyl)propanoate
  • Benzenepropanoic acid, α-ethoxy-4-hydroxy-, ethyl ester, (αS)-
  • Benzenepropanoic acid, .alpha.-ethoxy-4-hydroxy-, ethyl ester, (.alpha.S)-
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