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Atomfair Vinyl 4-(1,1-dimethylethyl)benzoate C13H16O2

Description Vinyl 4-(1,1-dimethylethyl)benzoate (CAS No. 15484-80-7) is a high-purity specialty ester with the molecular formula C13H16O2. Also known as ethenyl 4-tert-butylbenzoate , this compound features a reactive vinyl group adjacent to a sterically hindered tert-butyl-substituted aromatic ring, making it valuable for controlled polymerization and functional material synthesis. Its unique structure enables applications in advanced polymer chemistry, surface modification, and specialty coatings. Supplied as a clear liquid with ??95% purity (GC), it is rigorously tested for consistency and stored under inert conditions to prevent premature polymerization. Ideal for researchers developing high-performance resins, adhesives, or photoresists requiring tailored reactivity profiles.

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Description

Description

Vinyl 4-(1,1-dimethylethyl)benzoate (CAS No. 15484-80-7) is a high-purity specialty ester with the molecular formula C13H16O2. Also known as ethenyl 4-tert-butylbenzoate, this compound features a reactive vinyl group adjacent to a sterically hindered tert-butyl-substituted aromatic ring, making it valuable for controlled polymerization and functional material synthesis. Its unique structure enables applications in advanced polymer chemistry, surface modification, and specialty coatings. Supplied as a clear liquid with ??95% purity (GC), it is rigorously tested for consistency and stored under inert conditions to prevent premature polymerization. Ideal for researchers developing high-performance resins, adhesives, or photoresists requiring tailored reactivity profiles.

  • CAS No: 15484-80-7
  • Molecular Formula: C13H16O2
  • Molecular Weight: 204.26
  • Exact Mass: 204.115029749
  • Monoisotopic Mass: 204.115029749
  • IUPAC Name: ethenyl 4-tert-butylbenzoate
  • SMILES: CC(C)(C)C1=CC=C(C=C1)C(=O)OC=C
  • Synonyms: 15484-80-7, Vinyl 4-(1,1-dimethylethyl)benzoate, EINECS 239-510-5, DTXSID40165748, DTXCID7088239

Application

Vinyl 4-(1,1-dimethylethyl)benzoate serves as a key monomer for synthesizing polymers with enhanced thermal stability due to its tert-butyl aromatic group. It is utilized in photo-crosslinkable coatings where the vinyl group enables UV-initiated curing. Researchers employ it to modify surface properties of materials through graft polymerization. The compound’s steric hindrance allows controlled radical polymerization in advanced resin formulations.

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