Description

1-(Naphthalen-2-yl)-2-(piperidin-1-yl)ethane-1,2-dione (CAS No. 128592-64-3) is a high-purity organic compound with the molecular formula C₁₇H₁₇NO₂. This naphthalene-derived diketone features a piperidine substitution, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. The compound exhibits a molecular weight of 267.32 g/mol and is characterized by its crystalline solid form under standard conditions. Its structural uniqueness lends itself to applications in ligand synthesis, heterocyclic chemistry, and as a building block for complex molecular architectures. Suitable for use in controlled laboratory environments, this product is rigorously tested for purity and consistency, ensuring reliable performance in research applications.

Properties

• CAS Number: 128592-64-3
• Complexity: 373
• IUPAC Name: 1-(2-naphthyl)-2-(1-piperidyl)ethane-1,2-dione
• InChI: InChI=1S/C17H17NO2/c19-16(17(20)18-10-4-1-5-11-18)15-9-8-13-6-2-3-7-14(13)12-15/h2-3,6-9,12H,1,4-5,10-11H2
• InChI Key: MNRAHQSWKBGJII-UHFFFAOYSA-N
• Exact Mass: 267.125928785
• Molecular Formula: C17H17NO2
• Molecular Weight: 267.32
• SMILES: C1CCN(CC1)C(=O)C(=O)C2=CC3=CC=CC=C3C=C2
• Topological: 37.4
• Monoisotopic Mass: 267.125928785
• Synonyms: 128592-64-3, 1-(naphthalen-2-yl)-2-(piperidin-1-yl)ethane-1,2-dione, starbld0037562, DB-126499, 1-(2-Naphthalenyl)-2-(1-piperidinyl)-1,2-ethanedione

Application

1-(Naphthalen-2-yl)-2-(piperidin-1-yl)ethane-1,2-dione is primarily utilized as a key intermediate in the synthesis of pharmacologically active compounds, particularly in the development of heterocyclic frameworks. Its diketone functionality enables participation in condensation and cyclization reactions, making it valuable for constructing complex organic molecules. Researchers also employ this compound in metal-chelating studies due to its potential coordination sites. Additionally, it serves as a precursor in materials science for designing organic electronic components.

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