N-(S)-Glycidylphthalimide

• CAT Number: R039697
• CAS Number: 161596-47-0
• Molecular Formula: C11H9NO3
• Molecular Weight: 203.19
• Purity: ≥95%
• Synonyms: (S)-2-(Oxiran-2-ylmethyl)-1H-isoindole-1,3(2H)-dione; (S)-2-[(Oxiranyl)methyl]isoindole-1,3-dione; (S)-N-(2,3-Epoxypropan-1-yl)phthalimide; (S)-N-(2,3-Epoxypropyl)phthalimide; 2-[(S)-2-Oxiranylmethyl]-1H-isoindol-1,3(2H)-dione; N-((2S)-Oxiran-2-ylmet
• Storage: Room temperature
• IUPAC Name: 2-[[(2S)-oxiran-2-yl]methyl]isoindole-1,3-dione
• InChI: InChI=1S/C11H9NO3/c13-10-8-3-1-2-4-9(8)11(14)12(10)5-7-6-15-7/h1-4,7H,5-6H2/t7-/m0/s1
• InChIKey: DUILGEYLVHGSEE-ZETCQYMHSA-N
• SMILES: C1[C@@H](O1)CN2C(=O)C3=CC=CC=C3C2=O

N-(S)-Glycidylphthalimide（Cat No.:R039697）is a chiral epoxide-containing compound derived from phthalimide and (S)-glycidol. It features a phthalimide moiety attached to a glycidyl (epoxypropyl) group with defined (S)-stereochemistry, making it useful in asymmetric synthesis. The strained epoxide ring is highly reactive, enabling nucleophilic ring-opening reactions with various amines, thiols, or alcohols. N-(S)-Glycidylphthalimide is commonly used as a chiral intermediate or linker in the synthesis of pharmaceuticals, peptides, and polymeric materials. Its dual functionality—aromatic imide and epoxide—offers versatility for selective modification in both research and industrial applications.