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CS-W001157 4
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3-Ethylbicyclo[3.2.0]hept-3-en-6-one

  • CAS No. 1235479-59-0

  • Cat. No. CS-0375871
  • Purity≥98%
  • MDL No.MFCD24713107

*For research and further manufacturing use only, not for direct human use.

3-Ethylbicyclo[3.2.0]hept-3-en-6-one|CS-0375871

Structure of 1235479-59-0

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General Information

  • CAS No. 1235479-59-0
  • Cat. No. CS-0375871
  • Purity ≥98%
  • MDL No. MFCD24713107
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₁₂O
  • Molecular Weight 136.19
  • Synonym(s) 3-Ethylbicyclo[3.2.0]hept-3-ene-6-one
  • SMILES O=C1C2C=C(CC)CC2C1

Description

3-Ethylbicyclo[3.2.0]hept-3-en-6-one features a strained bicyclic framework with a conjugated enone system, enabling efficient Diels-Alder cycloadditions. The ethyl substituent at the bridgehead position enhances regiochemical control in asymmetric synthesis, while the ketone moiety serves as a handle for selective functionalization. This structure combines high reactivity with predictable stereochemical outcomes.

Application

3-Ethylbicyclo[3.2.0]hept-3-en-6-one serves as a versatile bicyclic enone scaffold for synthetic applications in natural product and medicinal chemistry. Its conjugated enone system enables reliable Michael additions, Diels–Alder cycloadditions, and functionalization at the C3 position. Bench-stable and readily purified by flash chromatography, it functions as a key building block for complex terpene-like architectures and heterocyclic systems requiring defined stereochemistry and ring strain.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H227-H315-H319-H335
Precautionary Statements : P210-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P403-P405-P501

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Computational Chemistry Data

  • TPSA   17.07
  • LogP   1.9317
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   1

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