Atomfair Cyclohex-3-en-1-one C6H8O

Description Cyclohex-3-en-1-one (CAS No. 4358-63-8) is a cyclic unsaturated ketone with the molecular formula C6H8O . This high-purity organic compound is widely utilized in synthetic chemistry, pharmaceuticals, and material science due to its reactive enone functionality. Its IUPAC name, cyclohex-3-en-1-one , reflects its structural features: a six-membered ring with a double bond at the 3-position and a carbonyl group at the 1-position. Available in various quantities, our product undergoes rigorous quality control to ensure >98% purity (GC), making it ideal for research and industrial applications. Store in a cool, dry place under inert conditions to maintain stability.

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Description

Description

Cyclohex-3-en-1-one (CAS No. 4358-63-8) is a cyclic unsaturated ketone with the molecular formula C6H8O. This high-purity organic compound is widely utilized in synthetic chemistry, pharmaceuticals, and material science due to its reactive enone functionality. Its IUPAC name, cyclohex-3-en-1-one, reflects its structural features: a six-membered ring with a double bond at the 3-position and a carbonyl group at the 1-position. Available in various quantities, our product undergoes rigorous quality control to ensure >98% purity (GC), making it ideal for research and industrial applications. Store in a cool, dry place under inert conditions to maintain stability.

  • CAS No: 4358-63-8
  • Molecular Formula: C6H8O
  • Molecular Weight: 96.13
  • Exact Mass: 96.057514874
  • Monoisotopic Mass: 96.057514874
  • IUPAC Name: cyclohex-3-en-1-one
  • SMILES: C1CC(=O)CC=C1
  • Synonyms: Cyclohex-3-en-1-one, 3-Cyclohexen-1-one, 4096-34-8, Cyclohex-3-enone, EINECS 223-850-6

Application

Cyclohex-3-en-1-one serves as a versatile intermediate in organic synthesis, particularly in Diels-Alder reactions and Michael additions. It is employed in the production of fragrances, agrochemicals, and pharmaceutical precursors. Researchers also utilize it to study ring-opening polymerization and catalytic hydrogenation processes.

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