Description

1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl 2-methoxyacetate (CAS No. 2248345-93-7) is a high-purity organic compound with the molecular formula C₁₁H₉NO₅, widely utilized in pharmaceutical and chemical research. This compound features a reactive isoindole-1,3-dione (phthalimide) core functionalized with a 2-methoxyacetate ester group, making it a versatile intermediate for synthetic applications. Its IUPAC name, (1,3-dioxoisoindol-2-yl) 2-methoxyacetate, reflects its precise structural configuration. Suitable for laboratory use, this product is rigorously tested for quality, ensuring optimal performance in coupling reactions, polymer chemistry, and medicinal chemistry studies. Available in various quantities, it is ideal for researchers seeking reliable and well-characterized building blocks for complex organic synthesis.

Properties

• CAS Number: 2248345-93-7
• Complexity: 330
• IUPAC Name: (1,3-dioxoisoindolin-2-yl) 2-methoxyacetate
• InChI: InChI=1S/C11H9NO5/c1-16-6-9(13)17-12-10(14)7-4-2-3-5-8(7)11(12)15/h2-5H,6H2,1H3
• InChI Key: RGIHCQWIRIDSDQ-UHFFFAOYSA-N
• Exact Mass: 235.04807239
• Molecular Formula: C11H9NO5
• Molecular Weight: 235.19
• SMILES: COCC(=O)ON1C(=O)C2=CC=CC=C2C1=O
• Topological: 72.9
• Monoisotopic Mass: 235.04807239
• Synonyms: EN300-6513125, 1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl 2-methoxyacetate, 2248345-93-7

Application

1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl 2-methoxyacetate serves as a key intermediate in the synthesis of phthalimide-derived compounds, which are pivotal in drug discovery and material science. Its reactive ester moiety enables efficient acylation reactions, facilitating the development of novel bioactive molecules. Researchers also employ this compound in polymer modification studies due to its ability to introduce functional groups into polymeric matrices. Additionally, it is explored in the design of photoactive materials and as a precursor for heterocyclic scaffolds in medicinal chemistry.

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