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Atomfair 6-(4-Hydroxyphenoxy)hexyl prop-2-enoate C15H20O4

Description 6-(4-Hydroxyphenoxy)hexyl prop-2-enoate (CAS No. 161841-12-9) is a specialized acrylate ester with a molecular formula of C15H20O4. This high-purity compound features a unique structure combining a hydroxyphenoxy group with a hexyl acrylate moiety, making it highly valuable for advanced polymer synthesis and material science applications. Its reactive acrylate group enables facile incorporation into polymer backbones, while the hydroxyphenoxy segment provides additional functionality for crosslinking or further modification. Supplied as a clear to pale yellow liquid, this compound is rigorously tested for quality and consistency, ensuring optimal performance in demanding research environments. Ideal for developing specialty adhesives, coatings, or functionalized polymers…

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Description

Description

6-(4-Hydroxyphenoxy)hexyl prop-2-enoate (CAS No. 161841-12-9) is a specialized acrylate ester with a molecular formula of C15H20O4. This high-purity compound features a unique structure combining a hydroxyphenoxy group with a hexyl acrylate moiety, making it highly valuable for advanced polymer synthesis and material science applications. Its reactive acrylate group enables facile incorporation into polymer backbones, while the hydroxyphenoxy segment provides additional functionality for crosslinking or further modification. Supplied as a clear to pale yellow liquid, this compound is rigorously tested for quality and consistency, ensuring optimal performance in demanding research environments. Ideal for developing specialty adhesives, coatings, or functionalized polymers with tailored properties.

  • CAS No: 161841-12-9
  • Molecular Formula: C15H20O4
  • Molecular Weight: 264.32
  • Exact Mass: 264.13615911
  • Monoisotopic Mass: 264.13615911
  • IUPAC Name: 6-(4-hydroxyphenoxy)hexyl prop-2-enoate
  • SMILES: C=CC(=O)OCCCCCCOC1=CC=C(C=C1)O
  • Synonyms: 161841-12-9, 6-(4-Hydroxyphenoxy)hexyl acrylate, 6-(4-hydroxyphenoxy)hexyl prop-2-enoate, 2-Propenoic acid, 6-(4-hydroxyphenoxy)hexyl ester, 4-(6-ACRYLOXY-HEX-1-YL-OXY)PHENOL

Application

6-(4-Hydroxyphenoxy)hexyl prop-2-enoate serves as a key monomer in the synthesis of advanced polymeric materials, particularly for applications requiring UV-curable coatings with enhanced adhesion and chemical resistance. Its dual functionality makes it valuable for creating crosslinked networks in dental composites or biomedical hydrogels. Researchers also utilize this compound to develop specialty pressure-sensitive adhesives with tunable mechanical properties.

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