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Atomfair 1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl nonanoate C17H21NO4

Description 1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl nonanoate (CAS No. 2248328-91-6) is a high-purity organic compound with the molecular formula C17H21NO4. This specialized ester derivative features a phthalimide core linked to a nonanoate moiety, making it a valuable intermediate for synthetic organic chemistry and pharmaceutical research. With an IUPAC name of (1,3-dioxoisoindol-2-yl) nonanoate , this compound is characterized by its precise structural configuration and exceptional purity, ensuring reproducibility in advanced research applications. It is supplied in rigorously controlled batches, with analytical data (including1H NMR,13C NMR, and HPLC) available upon request. Ideal for medicinal chemistry, material science, and fine chemical synthesis, this product is packaged under…

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Description

Description

1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl nonanoate (CAS No. 2248328-91-6) is a high-purity organic compound with the molecular formula C17H21NO4. This specialized ester derivative features a phthalimide core linked to a nonanoate moiety, making it a valuable intermediate for synthetic organic chemistry and pharmaceutical research. With an IUPAC name of (1,3-dioxoisoindol-2-yl) nonanoate, this compound is characterized by its precise structural configuration and exceptional purity, ensuring reproducibility in advanced research applications. It is supplied in rigorously controlled batches, with analytical data (including 1H NMR, 13C NMR, and HPLC) available upon request. Ideal for medicinal chemistry, material science, and fine chemical synthesis, this product is packaged under inert conditions to guarantee stability and longevity.

  • CAS No: 2248328-91-6
  • Molecular Formula: C17H21NO4
  • Molecular Weight: 303.35
  • Exact Mass: 303.14705815
  • Monoisotopic Mass: 303.14705815
  • IUPAC Name: (1,3-dioxoisoindol-2-yl) nonanoate
  • SMILES: CCCCCCCCC(=O)ON1C(=O)C2=CC=CC=C2C1=O
  • Synonyms: 1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl nonanoate, 2248328-91-6, EN300-6514309

Application

1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl nonanoate serves as a versatile building block in the synthesis of phthalimide-based pharmaceuticals and agrochemicals. Its reactive ester group enables efficient acylation reactions, particularly in peptide coupling and polymer modification. Researchers utilize this compound in the development of prodrugs or controlled-release formulations due to its hydrolyzable linker. It may also function as a photoactive component in advanced material applications.

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