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Atomfair Allyl phenyl ether C9H10O

Description Allyl Phenyl Ether ( prop-2-enoxybenzene , CAS No. 1746-13-0) is a high-purity organic compound with the molecular formula C9H10O . This clear, colorless to pale yellow liquid is widely utilized in organic synthesis, fragrance formulation, and polymer chemistry due to its reactive allyl and phenyl functional groups. With a boiling point of approximately 191-192??C and a density of 0.98 g/cm3, it is soluble in common organic solvents like ethanol, ether, and acetone. Ideal for researchers, this compound is rigorously tested via GC, HPLC, and NMR to ensure ??98% purity. Packaged under inert gas in amber glass bottles to prevent…

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Description

Description

Allyl Phenyl Ether (prop-2-enoxybenzene, CAS No. 1746-13-0) is a high-purity organic compound with the molecular formula C9H10O. This clear, colorless to pale yellow liquid is widely utilized in organic synthesis, fragrance formulation, and polymer chemistry due to its reactive allyl and phenyl functional groups. With a boiling point of approximately 191-192??C and a density of 0.98 g/cm3, it is soluble in common organic solvents like ethanol, ether, and acetone. Ideal for researchers, this compound is rigorously tested via GC, HPLC, and NMR to ensure ??98% purity. Packaged under inert gas in amber glass bottles to prevent degradation. Handle with proper PPE in a well-ventilated environment.

  • CAS No: 1746-13-0
  • Molecular Formula: C9H10O
  • Molecular Weight: 134.17
  • Exact Mass: 134.073164938
  • Monoisotopic Mass: 134.073164938
  • IUPAC Name: prop-2-enoxybenzene
  • SMILES: C=CCOC1=CC=CC=C1
  • Synonyms: Allyl phenyl ether, (allyloxy)benzene, Phenyl allyl ether, Benzene, (2-propen-1-yloxy)-, (2-Propenyloxy)benzene

Application

Allyl phenyl ether serves as a versatile intermediate in Grignard reactions and allylic rearrangements. It is employed in the synthesis of flavoring agents, pharmaceuticals, and specialty polymers. Researchers also use it to study Claisen rearrangements due to its thermally labile allyl group. Its aromatic ether properties make it valuable in UV-curable resins and adhesives.

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