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.

Properties

• CAS Number: 2248328-91-6
• Complexity: 397
• IUPAC Name: (1,3-dioxoisoindolin-2-yl) nonanoate
• InChI: InChI=1S/C17H21NO4/c1-2-3-4-5-6-7-12-15(19)22-18-16(20)13-10-8-9-11-14(13)17(18)21/h8-11H,2-7,12H2,1H3
• InChI Key: GODYKGRHECSMAC-UHFFFAOYSA-N
• Exact Mass: 303.14705815
• Molecular Formula: C17H21NO4
• Molecular Weight: 303.35
• SMILES: CCCCCCCCC(=O)ON1C(=O)C2=CC=CC=C2C1=O
• Topological: 63.7
• Monoisotopic Mass: 303.14705815
• 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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