Description

2-(2,2,3,3,3-Pentafluoropropoxymethyl)oxirane (CAS No. 706-89-8) is a highly specialized fluorinated epoxy compound with the molecular formula C₆H₇F₅O₂. This organofluorine derivative features a reactive oxirane (epoxide) ring, making it a valuable intermediate in synthetic organic chemistry and materials science. The presence of the pentafluoropropoxymethyl group imparts unique physicochemical properties, including enhanced thermal stability, chemical resistance, and potential surface-modifying characteristics. This compound is supplied as a high-purity liquid suitable for research and industrial applications requiring fluorinated building blocks. Typical purity grades available: ≥95% (GC), with custom purity options upon request. Store under inert atmosphere at recommended temperatures to maintain stability.

Properties

• CAS Number: 706-89-8
• Complexity: 178
• IUPAC Name: 2-(2,2,3,3,3-pentafluoropropoxymethyl)oxirane
• InChI: InChI=1S/C6H7F5O2/c7-5(8,6(9,10)11)3-12-1-4-2-13-4/h4H,1-3H2
• InChI Key: ABTNQISXTOWQTC-UHFFFAOYSA-N
• Exact Mass: 206.03662027
• Molecular Formula: C6H7F5O2
• Molecular Weight: 206.11
• SMILES: C1C(O1)COCC(C(F)(F)F)(F)F
• Topological: 21.8
• Monoisotopic Mass: 206.03662027
• Synonyms: 706-89-8, 2-(2,2,3,3,3-Pentafluoropropoxymethyl)oxirane, 2-[(2,2,3,3,3-pentafluoropropoxy)methyl]oxirane, 3-(2,2,3,3,3-Pentafluoropropoxy)-1,2-propenoxide, 2,2,3,3,3-PENTAFLUOROPROPOXYLMETHYLOXIRANE, 3-(2,2,3,3,3-Pentafluoropropoxy)-1,2-propeneoxide, MFCD00054688, SCHEMBL1463851, DTXSID00476261, ABTNQISXTOWQTC-UHFFFAOYSA-N, SBB093584, AKOS016015585, DB-226898, 2-[(3,3,3,2,2-pentafluoropropoxy)methyl]oxirane, 2,2,3,3,3-pentafluoro-1-(oxiran-2-ylmethoxy)propane

Application

This fluorinated epoxide serves as a key precursor in the synthesis of advanced fluoropolymers and surface-modifying agents. Researchers utilize it to develop materials with enhanced chemical resistance and low surface energy properties. The compound finds application in specialty coatings, hydrophobic materials, and as a building block in pharmaceutical intermediates. Its unique structure allows for ring-opening reactions to create polyether-based fluorinated materials.

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