Description
1,4-Phenylene bis(4-((11-(acryloyloxy)undecyl)oxy)benzoate) (CAS No. 132900-74-4) is a high-purity, synthetic organic compound with the molecular formula C48H62O10. This specialized monomer features a rigid 1,4-phenylene core symmetrically functionalized with two acrylate-terminated undecoxybenzoate arms, making it an ideal crosslinking agent or reactive intermediate for advanced polymer synthesis. Its extended spacer chains (11-undecoxy) provide exceptional flexibility while maintaining liquid crystalline properties, enabling precise tuning of material properties in photoresists, optical films, and anisotropic networks. With a molecular weight of 799.00 g/mol, this compound exhibits excellent thermal stability and is particularly valuable for creating highly ordered mesogenic structures in liquid crystal displays (LCDs) and smart materials. Supplied as a white to off-white crystalline powder with ≥95% purity (HPLC), it is packaged under inert gas to preserve reactivity of the terminal acrylate groups. Suitable for research in advanced material science, photopolymerization studies, and functional polymer development.
Properties
- CAS Number: 132900-74-4
- Complexity: 1040
- IUPAC Name: [4-[4-(11-prop-2-enoyloxyundecoxy)benzoyl]oxyphenyl] 4-(11-prop-2-enoyloxyundecoxy)benzoate
- InChI: InChI=1S/C48H62O10/c1-3-45(49)55-37-21-17-13-9-5-7-11-15-19-35-53-41-27-23-39(24-28-41)47(51)57-43-31-33-44(34-32-43)58-48(52)40-25-29-42(30-26-40)54-36-20-16-12-8-6-10-14-18-22-38-56-46(50)4-2/h3-4,23-34H,1-2,5-22,35-38H2
- InChI Key: HKDFSVLZRLBYTD-UHFFFAOYSA-N
- Exact Mass: 798.43429817
- Molecular Formula: C48H62O10
- Molecular Weight: 799.0
- SMILES: C=CC(=O)OCCCCCCCCCCCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCCCCCCCCCCOC(=O)C=C
- Topological: 124
- Monoisotopic Mass: 798.43429817
- Synonyms: SCHEMBL12592433, AT43230, 1,4-PHENYLENE BIS(4-((11-(ACRYLOYLOXY)UNDECYL)OXY)BENZOATE), 132900-74-4
Application
This bifunctional acrylate monomer is primarily employed in the development of liquid crystalline elastomers and shape-memory polymers, where its rigid-rod structure induces anisotropic mechanical properties. Researchers utilize it as a crosslinker in photo-polymerizable systems for holographic data storage due to its ability to form ordered networks upon UV irradiation. The compound also serves as a key building block in synthesizing side-chain liquid crystal polymers for electro-optic applications, including tunable diffraction gratings and optical compensators. Its long flexible spacers make it particularly useful for studying the decoupling of mesogen mobility from polymer backbone effects in advanced material formulations.
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