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Atomfair 3a,4,5,6,7,7a-Hexahydro-4,7-methano-1H-inden-6-yl butyrate C14H20O2

Description 3a,4,5,6,7,7a-Hexahydro-4,7-methano-1H-inden-6-yl butyrate (CAS: 113889-23-9) is a high-purity synthetic ester compound with the molecular formula C14H20O2. This specialized chemical, also known by its IUPAC name 8-tricyclo[5.2.1.02,6]dec-3-enyl butanoate , features a unique tricyclic structure that makes it valuable for advanced organic synthesis and fragrance applications. The compound is supplied as a clear, colorless to pale yellow liquid with a characteristic ester-like odor. It is rigorously tested for purity and consistency, making it ideal for research in terpene derivatives, flavor/fragrance chemistry, and material science. Proper storage under inert atmosphere at 2-8??C is recommended to maintain stability.

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Description

Description

3a,4,5,6,7,7a-Hexahydro-4,7-methano-1H-inden-6-yl butyrate (CAS: 113889-23-9) is a high-purity synthetic ester compound with the molecular formula C14H20O2. This specialized chemical, also known by its IUPAC name 8-tricyclo[5.2.1.02,6]dec-3-enyl butanoate, features a unique tricyclic structure that makes it valuable for advanced organic synthesis and fragrance applications. The compound is supplied as a clear, colorless to pale yellow liquid with a characteristic ester-like odor. It is rigorously tested for purity and consistency, making it ideal for research in terpene derivatives, flavor/fragrance chemistry, and material science. Proper storage under inert atmosphere at 2-8??C is recommended to maintain stability.

  • CAS No: 113889-23-9
  • Molecular Formula: C14H20O2
  • Molecular Weight: 220.31
  • Exact Mass: 220.146329876
  • Monoisotopic Mass: 220.146329876
  • IUPAC Name: 8-tricyclo[5.2.1.02,6]dec-3-enyl butanoate
  • SMILES: CCCC(=O)OC1CC2CC1C3C2C=CC3
  • Synonyms: 17511-61-4, 3a,4,5,6,7,7a-Hexahydro-4,7-methano-1H-inden-6-yl butyrate, 8-tricyclo[5.2.1.02,6]dec-3-enyl butanoate, EINECS 241-515-2, HVEOFLOFUBUHEQ-UHFFFAOYSA-N

Application

This compound serves as a key intermediate in the synthesis of complex fragrance molecules, particularly woody and amber notes. Researchers utilize it in studying structure-odor relationships in terpenoid derivatives. The rigid tricyclic framework makes it valuable for investigating sterically constrained ester chemistry. It may also find application in polymer modification studies due to its reactive double bond.

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