Description
[4-[2-(4-Propylphenyl)ethynyl]phenyl] prop-2-enoate (CAS: 185912-82-7) is a high-purity organic compound with the molecular formula C20H18O2. This specialized chemical features a prop-2-enoate (acrylate) group linked to a phenyl ring, which is further connected via an ethynyl bridge to a 4-propylphenyl moiety. Its unique structure makes it valuable for advanced research in organic synthesis, materials science, and polymer chemistry. This product is rigorously tested for purity and consistency, ensuring reliable performance in laboratory and industrial applications. Suitable for researchers and scientists requiring precision chemicals for photopolymerization studies, liquid crystal development, or as a building block for functional materials.
Properties
- CAS Number: 185912-82-7
- Complexity: 423
- IUPAC Name: [4-[2-(4-propylphenyl)ethynyl]phenyl] prop-2-enoate
- InChI: InChI=1S/C20H18O2/c1-3-5-16-6-8-17(9-7-16)10-11-18-12-14-19(15-13-18)22-20(21)4-2/h4,6-9,12-15H,2-3,5H2,1H3
- InChI Key: ZJOIGKYWAJEWJR-UHFFFAOYSA-N
- Exact Mass: 290.130679813
- Molecular Formula: C20H18O2
- Molecular Weight: 290.4
- SMILES: CCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C=C
- Topological: 26.3
- Monoisotopic Mass: 290.130679813
- Synonyms: 185912-82-7, SCHEMBL74647, DTXSID901338089, 4-[2-(4-Propylphenyl)ethynyl]phenyl 2-propenoate
This compound is primarily used as a monomer or intermediate in the synthesis of advanced polymers and liquid crystalline materials. Researchers utilize it in photopolymerization studies due to its acrylate functionality, enabling UV-curable coatings or adhesives. It may also serve as a precursor for organic electronic materials or as a crosslinking agent in specialty resins. Its rigid aromatic structure contributes to thermal stability in polymeric systems.
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