Atomfair 1-Phenyl-2-(piperidin-1-yl)ethane-1,2-dione C13H15NO2 CAS 14377-63-0

Description

1-Phenyl-2-(piperidin-1-yl)ethane-1,2-dione (CAS No. 14377-63-0) is a high-purity organic compound with the molecular formula C₁₃H₁₅NO₂. This diketone derivative features a phenyl group and a piperidine moiety, making it a versatile intermediate for synthetic organic chemistry and pharmaceutical research. Its IUPAC name, 1-phenyl-2-piperidin-1-ylethane-1,2-dione, reflects its precise structural configuration. The compound is supplied as a fine powder or crystalline solid with ≥95% purity (HPLC), ensuring consistency for laboratory and industrial applications. Ideal for use in ketone-based reactions, cross-coupling methodologies, and heterocyclic synthesis, this product is rigorously tested for quality, stability, and solvent compatibility. Store in a cool, dry place under inert conditions to maintain optimal shelf life.

Properties

• CAS Number: 14377-63-0
• Complexity: 263
• IUPAC Name: 1-phenyl-2-(1-piperidyl)ethane-1,2-dione
• InChI: InChI=1S/C13H15NO2/c15-12(11-7-3-1-4-8-11)13(16)14-9-5-2-6-10-14/h1,3-4,7-8H,2,5-6,9-10H2
• InChI Key: BWSCMJUJHSJAEV-UHFFFAOYSA-N
• Exact Mass: 217.110278721
• Molecular Formula: C13H15NO2
• Molecular Weight: 217.26
• SMILES: C1CCN(CC1)C(=O)C(=O)C2=CC=CC=C2
• Topological: 37.4
• Monoisotopic Mass: 217.110278721
• Synonyms: 14377-63-0, 1-phenyl-2-(piperidin-1-yl)ethane-1,2-dione, 2-oxo-1-phenyl-2-piperidin-1-ylethanone, Piperidine, 1-(oxophenylacetyl)- (9CI), 1-phenyl-2-piperidin-1-ylethane-1,2-dione, 1,2-Ethanedione, 1-phenyl-2-(1-piperidinyl)-, 1-(phenylglyoxylyl)piperidine, MFCD19317614, SCHEMBL5564719, BWSCMJUJHSJAEV-UHFFFAOYSA-N, AKOS022345372, BS-4252, 1-piperidino-2-phenylethane-1,2-dione, DB-126969, W12906

Application

1-Phenyl-2-(piperidin-1-yl)ethane-1,2-dione serves as a key building block in the synthesis of bioactive molecules, particularly in medicinal chemistry for the development of CNS-targeting compounds. Its diketone structure enables participation in cyclization reactions to form pyrrole or pyridine derivatives. Researchers also utilize it as a precursor for ligands in catalytic systems or as a scaffold for probing enzyme inhibition mechanisms.

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