Description

4-Acetylamino-2-(diallylamino)anisole (CAS No. 51868-45-2) is a high-purity organic compound with the molecular formula C₁₅H₂₀N₂O₂. This specialized chemical, also known by its IUPAC name N-[3-[bis(prop-2-enyl)amino]-4-methoxyphenyl]acetamide, features a unique molecular structure combining acetyl, diallylamino, and methoxy functional groups. Our product is rigorously tested to ensure ≥95% purity (HPLC) and is supplied as a crystalline solid with excellent stability under recommended storage conditions (2-8°C in inert atmosphere). Ideal for pharmaceutical research and organic synthesis applications, this compound serves as a valuable intermediate in the development of novel bioactive molecules. Each batch is accompanied by comprehensive analytical data including ¹H NMR, HPLC chromatograms, and mass spectrometry results to guarantee quality and consistency for your research needs.

Properties

• CAS Number: 51868-45-2
• Complexity: 307
• IUPAC Name: N-[3-(diallylamino)-4-methoxy-phenyl]acetamide
• InChI: InChI=1S/C15H20N2O2/c1-5-9-17(10-6-2)14-11-13(16-12(3)18)7-8-15(14)19-4/h5-8,11H,1-2,9-10H2,3-4H3,(H,16,18)
• InChI Key: GGUYNLUBFGZIKN-UHFFFAOYSA-N
• Exact Mass: 260.152477885
• Molecular Formula: C15H20N2O2
• Molecular Weight: 260.33
• SMILES: CC(=O)NC1=CC(=C(C=C1)OC)N(CC=C)CC=C
• Topological: 41.6
• Monoisotopic Mass: 260.152477885
• Synonyms: 51868-45-2, 4-Acetylamino-2-(diallylamino)anisole, N-[3-[bis(prop-2-enyl)amino]-4-methoxyphenyl]acetamide, N-(3-(Diallylamino)-4-methoxyphenyl)acetamide, 3-(N,N-Diallyl)amino-4-methoxyacetanilide, SCHEMBL9327923, DTXSID80402740, GGUYNLUBFGZIKN-UHFFFAOYSA-N, AKOS015890511, DB-052038, 4-Acetylamino-2-(diallylamino)anisole, 97%

Application

4-Acetylamino-2-(diallylamino)anisole finds application as a key intermediate in medicinal chemistry research, particularly in the synthesis of potential therapeutic agents targeting neurological disorders. The compound’s unique structure makes it valuable for studying structure-activity relationships in drug discovery programs. Researchers utilize this chemical in the development of novel aniline derivatives with potential pharmacological activity. Its reactive diallylamino group allows for further functionalization through various organic transformations.

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