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CAS 40856-59-5

:

(S)-(-)-alpha-(Boc-Amino)-gamma-butyrolactone

Description:
(S)-(-)-alpha-(Boc-Amino)-gamma-butyrolactone, with the CAS number 40856-59-5, is a chiral compound that belongs to the class of gamma-butyrolactones. This substance features a butyrolactone ring, which is a cyclic ester, and contains a tert-butyloxycarbonyl (Boc) protecting group attached to an amino group. The presence of the Boc group indicates that this compound is often used in peptide synthesis and other organic synthesis applications, as it can protect the amino functionality during various chemical reactions. The (S)-(-) designation signifies that the compound has a specific stereochemistry, which is crucial for its biological activity and interactions. Typically, compounds like this exhibit moderate solubility in organic solvents and may have specific reactivity patterns due to the functional groups present. Its applications can extend to pharmaceuticals, where it may serve as an intermediate in the synthesis of biologically active molecules. As with many chiral compounds, the enantiomeric purity can significantly influence the compound's properties and efficacy in various applications.
Formula:C9H15NO4
InChI:InChI=1/C9H15NO4/c1-9(2,3)14-8(12)10-6-4-5-13-7(6)11/h6H,4-5H2,1-3H3,(H,10,12)/t6-/m0/s1
SMILES:CC(C)(C)OC(=N[C@H]1CCOC1=O)O
Synonyms:
  • carbamic acid, N-[(3S)-tetrahydro-2-oxo-3-furanyl]-, 1,1-dimethylethyl ester
  • tert-Butyl [(3S)-2-oxotetrahydrofuran-3-yl]carbamate
  • Boc-L-homoserine lactone
  • (S)-(-)-α-(N-t-BOC-Amino)-γ-butyrolactone
  • Boc-Hsl
  • (S)-(-)-alpha-(N-Boc-amino)-gamma-butyrolactone
  • (S)-tert-butyl 2-oxo-tetrahydrofuran-3-ylcarbamate
  • Boc-HoMoser lactone
  • (S)-(-)-α-(Boc-AMino)-γ-butyrolactone
  • (S)-(-)-alpha-(N-t-boc-Amino)-b-butyrolactone
  • See more synonyms
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