Description

4-Methoxy-3-[3-(4-methylpiperazin-1-yl)propoxy]aniline (CAS No. 846023-55-0) is a high-purity organic compound with the molecular formula C₁₅H₂₅N₃O₂. This aniline derivative features a methoxy-substituted aromatic ring linked to a 4-methylpiperazine moiety via a propoxy spacer, making it a valuable intermediate in pharmaceutical and biochemical research. Its well-defined structure and reactivity enable applications in drug discovery, particularly in the synthesis of kinase inhibitors and receptor-targeting molecules. Suitable for researchers requiring precise chemical modifications, this compound is supplied with comprehensive analytical data (including ¹H NMR, HPLC, and MS) to ensure quality and reproducibility. Store under inert conditions at -20°C for long-term stability.

Properties

• CAS Number: 846023-55-0
• Complexity: 270
• IUPAC Name: 4-methoxy-3-[3-(4-methylpiperazin-1-yl)propoxy]aniline
• InChI: InChI=1S/C15H25N3O2/c1-17-7-9-18(10-8-17)6-3-11-20-15-12-13(16)4-5-14(15)19-2/h4-5,12H,3,6-11,16H2,1-2H3
• InChI Key: DDWYYSNSEJHVFI-UHFFFAOYSA-N
• Exact Mass: 279.19467705
• Molecular Formula: C15H25N3O2
• Molecular Weight: 279.38
• SMILES: CN1CCN(CC1)CCCOC2=C(C=CC(=C2)N)OC
• Topological: 51
• Monoisotopic Mass: 279.19467705
• Synonyms: 846023-55-0, 4-Methoxy-3-(3-(4-methyl-1-piperazinyl)propoxy)benzenamine, 4-Methoxy-3-[3-(4-methyl-1-piperazinyl)propoxy]benzenamine, 4-METHOXY-3-(3-(4-METHYLPIPERAZIN-1-YL)PROPOXY)ANILINE, 4-Methoxy-3-[3-(4-methylpiperazin-1-yl)propoxy]aniline, Benzenamine, 4-methoxy-3-[3-(4-methyl-1-piperazinyl)propoxy]-, SCHEMBL5103081, DTXSID20730817, DDWYYSNSEJHVFI-UHFFFAOYSA-N, AKOS027255066, BS-17715, DB-349447, CS-0151067, 4-methoxy-3-[3-(4-methyl-piperazin-1-yl)-propoxy]-phenylamine

Application

This compound serves as a key building block in medicinal chemistry, particularly for developing kinase inhibitors due to its piperazine and aniline pharmacophores. Researchers utilize it in structure-activity relationship (SAR) studies to optimize drug candidates targeting neurodegenerative diseases or cancer. Its propoxy linker enhances solubility, facilitating in vitro assays. The methoxy group further allows selective functionalization for analog synthesis.

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