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Atomfair 13-Oxabicyclo[10.1.0]tridecane C12H22O

Description 13-Oxabicyclo[10.1.0]tridecane (CAS: 29540-84-9) is a high-purity cyclic organic compound with the molecular formula C12H22O . This epoxide derivative of cyclododecane features a strained three-membered oxirane ring fused to a 12-membered cycloalkane, making it a valuable intermediate in synthetic organic chemistry and materials science. Its unique bicyclic structure offers reactivity for ring-opening polymerizations, crosslinking reactions, and as a precursor for specialty chemicals. Available in research quantities, this compound is rigorously tested for purity and consistency, ensuring reliable performance in demanding applications. Suitable for use in pharmaceutical synthesis, polymer modification, and advanced material development.

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Description

Description

13-Oxabicyclo[10.1.0]tridecane (CAS: 29540-84-9) is a high-purity cyclic organic compound with the molecular formula C12H22O. This epoxide derivative of cyclododecane features a strained three-membered oxirane ring fused to a 12-membered cycloalkane, making it a valuable intermediate in synthetic organic chemistry and materials science. Its unique bicyclic structure offers reactivity for ring-opening polymerizations, crosslinking reactions, and as a precursor for specialty chemicals. Available in research quantities, this compound is rigorously tested for purity and consistency, ensuring reliable performance in demanding applications. Suitable for use in pharmaceutical synthesis, polymer modification, and advanced material development.

  • CAS No: 29540-84-9
  • Molecular Formula: C12H22O
  • Molecular Weight: 182.30
  • Exact Mass: 182.167065321
  • Monoisotopic Mass: 182.167065321
  • IUPAC Name: 13-oxabicyclo[10.1.0]tridecane
  • SMILES: C1CCCCCC2C(O2)CCCC1
  • Synonyms: 1,2-Epoxycyclododecane, 13-Oxabicyclo[10.1.0]tridecane, 286-99-7, CYCLODODECANE EPOXIDE, CCRIS 3754

Application

13-Oxabicyclo[10.1.0]tridecane is primarily used as a reactive intermediate in organic synthesis, particularly for ring-opening reactions to produce diols or polyether materials. Its strained epoxide ring enables crosslinking in polymer systems, enhancing thermal and mechanical properties. Researchers also employ it as a building block for macrocyclic compounds in supramolecular chemistry and catalysis.

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