Description

Allyl pentafluorophenyl ether (CAS No. 33104-02-8) is a high-purity fluorinated aromatic ether compound with the molecular formula C₉H₅F₅O. This specialized chemical, also known by its IUPAC name 1,2,3,4,5-pentafluoro-6-prop-2-enoxybenzene, features a reactive allyl group bonded to a pentafluorophenyl ring, making it a valuable intermediate in organofluorine chemistry. The presence of five fluorine atoms on the aromatic ring enhances its electron-withdrawing properties and stability under harsh conditions.

Our product is synthesized under strict quality control measures to ensure ≥98% purity (GC), with comprehensive analytical data including ¹H NMR, ¹⁹F NMR, and GC-MS spectra available upon request. The compound is supplied in amber glass bottles under inert atmosphere to maintain stability, with typical batch sizes ranging from 1g to 100g for research applications.

Key applications include use as:

• Precursor for fluorinated polymers and dendrimers
• Building block in pharmaceutical intermediates
• Crosslinking agent in specialty materials

Storage recommendation: Maintain at 2-8°C under nitrogen atmosphere. Shelf life of 24 months when stored properly.

Properties

• CAS Number: 33104-02-8
• Complexity: 209
• IUPAC Name: 1-allyloxy-2,3,4,5,6-pentafluoro-benzene
• InChI: InChI=1S/C9H5F5O/c1-2-3-15-9-7(13)5(11)4(10)6(12)8(9)14/h2H,1,3H2
• InChI Key: MYRHORGTVILPRU-UHFFFAOYSA-N
• Exact Mass: 224.02605559
• Molecular Formula: C9H5F5O
• Molecular Weight: 224.13
• SMILES: C=CCOC1=C(C(=C(C(=C1F)F)F)F)F
• Topological: 9.2
• Monoisotopic Mass: 224.02605559
• Synonyms: Allyl pentafluorophenyl ether, 33104-02-8, DTXSID50377815, DTXCID10328843, Allyloxypentafluorobenzene, 1,2,3,4,5-pentafluoro-6-prop-2-enoxybenzene, 1,2,3,4,5-pentafluoro-6-(prop-2-en-1-yloxy)benzene, Allyloxyperfluorobenzene, pentafluorophenyl allyl ether, SCHEMBL5954786, SBB096616, AKOS007930769, 1-(Allyloxy)-2,3,4,5,6-Pentafluorobenzene, 1,2,3,4,6-pentafluoro-5-prop-2-enyloxybenzene

Application

Allyl pentafluorophenyl ether serves as a versatile fluorinated building block in organic synthesis. Researchers utilize this compound for developing fluorinated liquid crystals with unique dielectric properties. In materials science, it functions as a crosslinker for creating high-performance fluoropolymers with enhanced thermal stability. The compound’s electron-deficient aromatic ring makes it particularly valuable in nucleophilic aromatic substitution reactions for pharmaceutical intermediate synthesis.

If you are interested or have any questions, please contact us at support@atomfair.com

Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.