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CAS 88790-38-9

:

1-Pyrrolidinecarboxylic acid, 2-(2-hydroxyethyl)-, 1,1-dimethylethylester, (S)-

Description:
1-Pyrrolidinecarboxylic acid, 2-(2-hydroxyethyl)-, 1,1-dimethylethyl ester, (S)-, is a chiral compound characterized by its pyrrolidine ring structure, which contributes to its unique chemical properties. This substance features a carboxylic acid moiety, an ester functional group, and a hydroxyethyl substituent, indicating its potential for various chemical reactivity and applications. The presence of the tert-butyl group enhances its stability and lipophilicity, making it suitable for use in pharmaceutical formulations. As a chiral molecule, it may exhibit different biological activities depending on its stereochemistry, which is crucial in drug development. The compound is likely to be soluble in organic solvents and may have moderate solubility in water due to the presence of the hydroxyethyl group. Its CAS number, 88790-38-9, allows for easy identification in chemical databases. Overall, this compound's structural features suggest potential utility in medicinal chemistry and related fields, particularly in the synthesis of biologically active molecules.
Formula:C11H21NO3
Synonyms:
  • (S)-1-Boc-2-(2-hydroxyethyl)pyrrolidine
  • Boc-(S)-2-(pyrrolidin-2-yl)ethan-1-ol 88790-38-9
  • Boc-(S)-2-(pyrrolidin-2-yl)ethan-1-ol
  • 1-Pyrrolidinecarboxylic acid, 2-(2-hydroxyethyl)-, 1,1-dimethylethyl ester, (2S)-
  • tert-butyl (2S)-2-(2-hydroxyethyl)pyrrolidine-1-carboxylate
  • tert-butyl (S)-2-(2-hydroxyethyl)pyrrolidine-1-carboxylate
  • 1-Pyrrolidinecarboxylic acid, 2-(2-hydroxyethyl)-, 1,1-dimethylethylester, (S)-
  • tert-Butyl (S)-2-(2-hydroxyethyl)pyrrolidine-1-carboxylate
  • (S)-tert-Butyl 2-(2-hydroxyethyl)pyrrolidine-1-carboxylate
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