Spiro[2.5]octane-5,7-dione

95%

  • Product Code: 76086
  CAS:    893411-52-4
Molecular Weight: 138.16 g./mol Molecular Formula: C₈H₁₀O₂
EC Number: MDL Number: MFCD11100381
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, sealed and dry
Product Description: Spiro[2.5]octane-5,7-dione is primarily utilized in organic synthesis as a versatile building block for constructing complex molecular frameworks. Its unique spirocyclic structure makes it valuable in the development of pharmaceuticals, particularly in the synthesis of bioactive compounds and drug intermediates. The compound’s diketone functionality allows it to participate in various chemical reactions, such as cyclizations and condensations, enabling the creation of diverse heterocyclic structures. Additionally, it is employed in materials science for designing novel polymers and organic materials with specific properties, such as enhanced stability or tailored reactivity. Its application extends to research settings, where it serves as a model compound for studying reaction mechanisms and exploring new synthetic pathways.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days $2,750.98
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1.000 10-20 days $7,645.36
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Spiro[2.5]octane-5,7-dione
Spiro[2.5]octane-5,7-dione is primarily utilized in organic synthesis as a versatile building block for constructing complex molecular frameworks. Its unique spirocyclic structure makes it valuable in the development of pharmaceuticals, particularly in the synthesis of bioactive compounds and drug intermediates. The compound’s diketone functionality allows it to participate in various chemical reactions, such as cyclizations and condensations, enabling the creation of diverse heterocyclic structures. Additionally, it is employed in materials science for designing novel polymers and organic materials with specific properties, such as enhanced stability or tailored reactivity. Its application extends to research settings, where it serves as a model compound for studying reaction mechanisms and exploring new synthetic pathways.
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