Description

Methyl 3-(2-(1,3-dioxoisoindolin-2-yl)ethyl)-6-fluoro-1H-indole-4-carboxylate (CAS No. 1408282-25-6) is a high-purity fluorinated indole derivative designed for advanced research and pharmaceutical applications. With the molecular formula C₂₀H₁₅FN₂O₄, this compound features a unique structural combination of an indole core, a phthalimide moiety, and a fluoro-substituent, making it a valuable intermediate in medicinal chemistry and drug discovery. It is supplied as a fine powder with ≥95% purity (HPLC), ensuring consistency for synthetic and biological studies. Proper storage at 2-8°C in a tightly sealed container is recommended to maintain stability. This product is intended for research purposes only and is not for human or veterinary use.

Properties

• CAS Number: 1408282-25-6
• Complexity: 603
• IUPAC Name: methyl 3-[2-(1,3-dioxoisoindolin-2-yl)ethyl]-6-fluoro-1H-indole-4-carboxylate
• InChI: InChI=1S/C20H15FN2O4/c1-27-20(26)15-8-12(21)9-16-17(15)11(10-22-16)6-7-23-18(24)13-4-2-3-5-14(13)19(23)25/h2-5,8-10,22H,6-7H2,1H3
• InChI Key: FFASSIQWTSNOTM-UHFFFAOYSA-N
• Exact Mass: 366.10158513
• Molecular Formula: C20H15FN2O4
• Molecular Weight: 366.3
• SMILES: COC(=O)C1=C2C(=CC(=C1)F)NC=C2CCN3C(=O)C4=CC=CC=C4C3=O
• Topological: 79.5
• Monoisotopic Mass: 366.10158513
• Synonyms: 1408282-25-6, Methyl 3-(2-(1,3-dioxoisoindolin-2-yl)ethyl)-6-fluoro-1H-indole-4-carboxylate, 1H-Indole-4-carboxylic acid, 3-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethyl]-6-fluoro-, methyl ester, methyl 3-[2-(1,3-dioxoisoindol-2-yl)ethyl]-6-fluoro-1H-indole-4-carboxylate, methyl 3-[2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)ethyl]-6-fluoro-1H-indole-4-carboxylate, C20H15FN2O4, 3-(2-(phthalimido)ethyl)-6-fluoro-1H-indole-4-carboxylic acid methyl ester, SCHEMBL20692464, AKOS030525442, 3-[2-(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)ethyl]-6-fluoro-1H-indole-4-carboxylic acid methyl ester, BS-15353, DB-228279, CS-0198930, D83642, Methyl3-(2-(1,3-dioxoisoindolin-2-yl)ethyl)-6-fluoro-1H-indole-4-carboxylate

Application

This compound serves as a key synthetic intermediate in the development of novel indole-based pharmaceuticals, particularly in kinase inhibitor research. Its fluorinated indole scaffold is useful for probing structure-activity relationships in drug design. Researchers may employ it in the synthesis of potential anticancer or anti-inflammatory agents due to its dual functional group compatibility.

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