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Atomfair 1,3-Dioxoisoindolin-2-yl hexanoate C14H15NO4

Description 1,3-Dioxoisoindolin-2-yl hexanoate (CAS No. 2170596-50-4) is a high-purity organic compound with the molecular formula C14H15NO4and IUPAC name (1,3-dioxoisoindol-2-yl) hexanoate . This specialized chemical features a phthalimide core esterified with hexanoic acid, offering unique reactivity for synthetic applications. Our product is rigorously characterized by HPLC, NMR, and mass spectrometry to ensure ??95% purity, packaged under inert atmosphere for maximum stability. Ideal for pharmaceutical intermediates, polymer chemistry, and materials science research. Available in research (100mg-1g) and bulk (5g-100g) quantities with optional analytical certificates. CAS: 2170596-50-4 Molecular Weight: 261.27 g/mol Synonyms: SCHEMBL3676598, DB-374614 Storage: -20??C under argon Handling: Moisture-sensitive

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Description

Description

1,3-Dioxoisoindolin-2-yl hexanoate (CAS No. 2170596-50-4) is a high-purity organic compound with the molecular formula C14H15NO4 and IUPAC name (1,3-dioxoisoindol-2-yl) hexanoate. This specialized chemical features a phthalimide core esterified with hexanoic acid, offering unique reactivity for synthetic applications. Our product is rigorously characterized by HPLC, NMR, and mass spectrometry to ensure ??95% purity, packaged under inert atmosphere for maximum stability. Ideal for pharmaceutical intermediates, polymer chemistry, and materials science research. Available in research (100mg-1g) and bulk (5g-100g) quantities with optional analytical certificates.

  • CAS: 2170596-50-4
  • Molecular Weight: 261.27 g/mol
  • Synonyms: SCHEMBL3676598, DB-374614
  • Storage: -20??C under argon
  • Handling: Moisture-sensitive
  • CAS No: 2170596-50-4
  • Molecular Formula: C14H15NO4
  • Molecular Weight: 261.27
  • Exact Mass: 261.10010796
  • Monoisotopic Mass: 261.10010796
  • IUPAC Name: (1,3-dioxoisoindol-2-yl) hexanoate
  • SMILES: CCCCCC(=O)ON1C(=O)C2=CC=CC=C2C1=O
  • Synonyms: 1,3-Dioxoisoindolin-2-yl hexanoate, 2170596-50-4, SCHEMBL3676598, DB-374614, EN300-6513175

Application

This compound serves as a versatile building block in organic synthesis, particularly for creating phthalimide-protected intermediates in peptide mimetics. The hexanoate ester moiety enables lipophilic modification of active pharmaceutical ingredients (APIs) to enhance bioavailability. Researchers utilize it in controlled-release formulations and as a precursor for functionalized polymers with tailored degradation profiles.

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