Description

Methyl 7-methyl-alpha-oxo-1H-indole-3-acetate (CAS No. 425640-13-7) is a high-purity organic compound with the molecular formula C₁₂H₁₁NO₃. This indole derivative, also known by its IUPAC name methyl 2-(7-methyl-1H-indol-3-yl)-2-oxoacetate, is a valuable intermediate in pharmaceutical and biochemical research. The compound features a reactive α-oxoester group attached to the 3-position of a 7-methylindole scaffold, making it useful for further synthetic modifications. Our product is rigorously tested for purity and consistency, ensuring optimal performance in your applications. Available in various quantities, this compound is ideal for researchers working on indole-based drug discovery, heterocyclic chemistry, and medicinal chemistry projects.

Properties

• CAS Number: 425640-13-7
• Complexity: 303
• IUPAC Name: methyl 2-(7-methyl-1H-indol-3-yl)-2-oxo-acetate
• InChI: InChI=1S/C12H11NO3/c1-7-4-3-5-8-9(6-13-10(7)8)11(14)12(15)16-2/h3-6,13H,1-2H3
• InChI Key: MHKYKAZMQYFAMW-UHFFFAOYSA-N
• Exact Mass: 217.07389321
• Molecular Formula: C12H11NO3
• Molecular Weight: 217.22
• SMILES: CC1=C2C(=CC=C1)C(=CN2)C(=O)C(=O)OC
• Topological: 59.2
• Monoisotopic Mass: 217.07389321
• Synonyms: 425640-13-7, Methyl 7-methyl-alpha-oxo-1H-indole-3-acetate, Methyl 2-(7-Methyl-3-indolyl)-2-oxoacetate, Methyl2-(7-Methyl-3-indolyl)-2-oxoacetate, 1H-Indole-3-acetic acid, 7-methyl-alpha-oxo-, methyl ester, Methyl 7-Methyl-?-oxo-1H-indole-3-acetic Acid Ester, MFCD12546263, methyl 2-(7-methyl-1H-indol-3-yl)-2-oxoacetate, SCHEMBL989756, (7-methyl-1H-indol-3-yl)oxoacetic acid methyl ester, 1h-indole-3-acetic acid,7-methyl-a-oxo-,methyl ester, MHKYKAZMQYFAMW-UHFFFAOYSA-N, DTXSID901271007, AC6126, SY058656, DB-327885, Methyl 7-methyl-I+/–oxo-1H-indole-3-acetate, (7 -Methyl-1H-indol-3-yl)-oxo-acetic acid methyl ester, (7-Methyl-1H-indol-3-yl)-oxo-acetic acid methyl ester, 1H-Indole-3-aceticacid,7-methyl-alpha-oxo-,methylester

Application

Methyl 7-methyl-alpha-oxo-1H-indole-3-acetate serves as a key synthetic intermediate in the preparation of biologically active indole derivatives. Researchers utilize this compound in the development of potential pharmaceutical agents targeting various disease pathways. Its reactive α-oxoester moiety allows for further functionalization, making it valuable for structure-activity relationship studies. The 7-methylindole core structure is of particular interest in medicinal chemistry due to its prevalence in many pharmacologically active compounds.

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