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Atomfair (S)-4-isopropyloxazolidine-2,5-dione C7H11NO3

Description (S)-4-isopropyloxazolidine-2,5-dione (CAS No. 3190-70-3) is a high-purity chiral oxazolidinedione derivative with the molecular formula C7H11NO3. This compound, also known by its IUPAC name 4-(2-methylpropyl)-1,3-oxazolidine-2,5-dione , is a valuable building block in organic synthesis and pharmaceutical research. It features a reactive oxazolidine-2,5-dione core, making it useful for asymmetric synthesis and as a precursor for bioactive molecules. Available in >98% purity (HPLC), this product is rigorously tested for quality, including chiral purity, and is supplied in sealed packaging under inert gas to ensure stability. Ideal for researchers developing enantioselective catalysts, peptidomimetics, or novel therapeutic agents.

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Description

Description

(S)-4-isopropyloxazolidine-2,5-dione (CAS No. 3190-70-3) is a high-purity chiral oxazolidinedione derivative with the molecular formula C7H11NO3. This compound, also known by its IUPAC name 4-(2-methylpropyl)-1,3-oxazolidine-2,5-dione, is a valuable building block in organic synthesis and pharmaceutical research. It features a reactive oxazolidine-2,5-dione core, making it useful for asymmetric synthesis and as a precursor for bioactive molecules. Available in >98% purity (HPLC), this product is rigorously tested for quality, including chiral purity, and is supplied in sealed packaging under inert gas to ensure stability. Ideal for researchers developing enantioselective catalysts, peptidomimetics, or novel therapeutic agents.

  • CAS No: 3190-70-3
  • Molecular Formula: C7H11NO3
  • Molecular Weight: 157.17
  • Exact Mass: 157.07389321
  • Monoisotopic Mass: 157.07389321
  • IUPAC Name: 4-(2-methylpropyl)-1,3-oxazolidine-2,5-dione
  • SMILES: CC(C)CC1C(=O)OC(=O)N1
  • Synonyms: EINECS 221-692-2, NSC 351903, 221-692-2, 4-Isobutyloxazolidine-2,5-dione, 51248-35-2

Application

(S)-4-isopropyloxazolidine-2,5-dione is primarily employed as a chiral auxiliary in asymmetric synthesis for the preparation of enantiomerically pure compounds. It serves as a key intermediate in the synthesis of non-proteinogenic amino acids and peptide analogs with potential biological activity. Researchers also utilize this compound in the development of enzyme inhibitors and as a scaffold for drug discovery targeting neurological disorders.

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