Description

2-Acetylcyclohexanone (CAS: 125117-37-5) is a high-purity cyclic ketone derivative with the molecular formula C₈H₁₂O₂. This compound, also known by its IUPAC name 2-acetylcyclohexan-1-one, features a cyclohexanone backbone substituted with an acetyl group at the 2-position, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its unique structure enables versatile reactivity, particularly in condensation and cyclization reactions.

Our 2-Acetylcyclohexanone is rigorously tested for purity and consistency, ensuring optimal performance in sensitive applications. It is supplied in sealed containers under inert conditions to maintain stability. Ideal for researchers in medicinal chemistry, catalysis, and materials science, this compound is a key building block for synthesizing complex heterocycles and fine chemicals.

Synonyms: 2-ACETYLCYCLOHEXANONE, 2-Acetyl-1-cyclohexanone, α-Acetylcyclohexanone

Properties

• CAS Number: 125117-37-5
• Complexity: 161
• IUPAC Name: 2-acetylcyclohexanone
• InChI: InChI=1S/C8H12O2/c1-6(9)7-4-2-3-5-8(7)10/h7H,2-5H2,1H3
• InChI Key: OEKATORRSPXJHE-UHFFFAOYSA-N
• Exact Mass: 140.083729621
• Molecular Formula: C8H12O2
• Molecular Weight: 140.18
• SMILES: CC(=O)C1CCCCC1=O
• Topological: 34.1
• Monoisotopic Mass: 140.083729621
• Synonyms: 2-ACETYLCYCLOHEXANONE, 874-23-7, 2-Acetyl-1-cyclohexanone, Cyclohexanone, 2-acetyl-, .alpha.-Acetylcyclohexanone, alpha-Acetylcyclohexanone, Acetylcyclohexanone, DTXSID0049365, NSC 7713, EINECS 212-858-5, AI3-19261, DTXCID7029324, 212-858-5, ethanone, 1-(2-hydroxy-1-cyclohexen-1-yl)-, inchi=1/c8h12o2/c1-6(9)7-4-2-3-5-8(7)10/h10h,2-5h2,1h, oekatorrspxjhe-uhfffaoysa-n, 2-acetylcyclohexan-1-one, 2-acetyl-cyclohexanone, 2-ACETYL CYCLOHEXANONE, 125117-37-5, MFCD00001633, 1-acetyl-2-oxocyclohexane, 424823-02-9, acetyl cyclohexanone, 2-Acetylcyclohexanone; 2-Acetyl-1-cyclohexanone; 2-Acetylcyclohexanone; NSC 7713; alpha-Acetylcyclohexanone, 2-acetyl-cyclohexan-1-one, SCHEMBL63339, 2-Acetylcyclohexanone, 97%, CHEMBL3187909, NSC7713, CS-D1351, NSC-7713, Tox21_202874, SBB056190, STL264116, AKOS005206863, FA10212, PB43660, NCGC00260420-01, AC-22529, CAS-874-23-7, SY039226, DB-076946, DB-364545, A0881, NS00039192, ST50823683, EN300-11786

Application

2-Acetylcyclohexanone serves as a critical precursor in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. It is widely used in the preparation of heterocyclic compounds, such as pyrazoles and pyrroles, through condensation reactions. Researchers also employ it in catalytic studies and as a ligand modifier in asymmetric synthesis. Its reactivity makes it valuable for exploring novel reaction pathways in organic chemistry.

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