Description

1,3-Dioxoisoindolin-2-yl heptanoate (CAS No. 2159068-51-4) is a high-purity synthetic organic compound with the molecular formula C₁₅H₁₇NO₄. This specialized ester derivative of isoindoline-1,3-dione is designed for advanced research applications, particularly in pharmaceutical and chemical synthesis. The compound features a heptanoate ester group attached to the nitrogen of the phthalimide core, offering unique reactivity for conjugation and derivatization.

Our product is synthesized under stringent quality control measures, ensuring >95% purity by HPLC analysis. It is supplied as a white to off-white crystalline powder, stable under recommended storage conditions (2-8°C in inert atmosphere). The molecular weight of 275.30 g/mol and precise structural characteristics make it particularly valuable for:

• Development of novel pharmaceutical intermediates
• Organic synthesis of functionalized isoindoline derivatives
• Materials science research
• Bioconjugation studies

Each batch is accompanied by comprehensive analytical data including ¹H NMR, ¹³C NMR, and mass spectrometry reports. Available in research quantities from 100mg to 10g scale, with custom synthesis options available for bulk requirements.

Properties

• CAS Number: 2159068-51-4
• Complexity: 369
• IUPAC Name: (1,3-dioxoisoindolin-2-yl) heptanoate
• InChI: InChI=1S/C15H17NO4/c1-2-3-4-5-10-13(17)20-16-14(18)11-8-6-7-9-12(11)15(16)19/h6-9H,2-5,10H2,1H3
• InChI Key: GASWUODIFYKJCL-UHFFFAOYSA-N
• Exact Mass: 275.11575802
• Molecular Formula: C15H17NO4
• Molecular Weight: 275.30
• SMILES: CCCCCCC(=O)ON1C(=O)C2=CC=CC=C2C1=O
• Topological: 63.7
• Monoisotopic Mass: 275.11575802
• Synonyms: 1,3-Dioxoisoindolin-2-yl heptanoate, 2159068-51-4, EN300-6513303, 1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl heptanoate

Application

1,3-Dioxoisoindolin-2-yl heptanoate serves as a versatile building block in organic synthesis, particularly for the preparation of phthalimide-protected intermediates. The compound’s reactive ester moiety enables efficient acylation reactions under mild conditions. Researchers utilize this chemical in the development of novel drug candidates, where its structural features facilitate controlled release mechanisms. The heptanoate chain provides enhanced lipid solubility for improved bioavailability studies in pharmacological research.

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.