Description
1,4-Phenylene bis(4-((acryloyloxy)methoxy)benzoate) (CAS: 123864-17-5) is a high-purity, specialty monomer designed for advanced polymer and material science applications. With the molecular formula C46H58O10, this compound features a rigid 1,4-phenylene core flanked by acrylate-functionalized benzoate groups, enabling crosslinking and photopolymerization in UV-curable resins, coatings, and adhesives. Its bifunctional structure ensures enhanced thermal stability, mechanical strength, and chemical resistance in polymer networks. Ideal for research and industrial use, this monomer is supplied with rigorous QC validation (HPLC, NMR) to guarantee >98% purity. Store under inert conditions (N2, -20°C) to prevent premature polymerization.
Properties
- CAS Number: 123864-17-5
- Complexity: 1040
- IUPAC Name: [4-[4-(3-methyl-9-prop-2-enoyloxy-nonoxy)benzoyl]oxyphenyl] 4-(3-methyl-9-prop-2-enoyloxy-nonoxy)benzoate
- InChI: InChI=1S/C46H58O10/c1-5-43(47)53-31-13-9-7-11-15-35(3)29-33-51-39-21-17-37(18-22-39)45(49)55-41-25-27-42(28-26-41)56-46(50)38-19-23-40(24-20-38)52-34-30-36(4)16-12-8-10-14-32-54-44(48)6-2/h5-6,17-28,35-36H,1-2,7-16,29-34H2,3-4H3
- InChI Key: IBYXBHRGDTUIBX-UHFFFAOYSA-N
- Exact Mass: 770.40299804
- Molecular Formula: C46H58O10
- Molecular Weight: 770.9
- SMILES: CC(CCCCCCOC(=O)C=C)CCOC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)OC(=O)C3=CC=C(C=C3)OCCC(C)CCCCCCOC(=O)C=C
- Topological: 124
- Monoisotopic Mass: 770.40299804
- Synonyms: 123864-17-5, 1,4-phenylene bis(4-((acryloyloxy)methoxy)benzoate), 1,4-Phenylene bis(4-((9-(acryloyloxy)-3-methylnonyl)oxy)benzoate), IBYXBHRGDTUIBX-UHFFFAOYSA-N, SCHEMBL29157750, 1,4-Phenylenebis(4-((9-(acryloyloxy)-3-methylnonyl)oxy)benzoate), [4-[4-(3-methyl-9-prop-2-enoyloxynonoxy)benzoyl]oxyphenyl] 4-(3-methyl-9-prop-2-enoyloxynonoxy)benzoate
This monomer is pivotal in synthesizing high-performance photopolymers for 3D printing (e.g., stereolithography) and optical coatings due to its rapid UV curing. It also serves as a crosslinker in liquid crystal displays (LCDs) to enhance alignment layer durability. Researchers leverage its dual acrylate groups for designing stimuli-responsive hydrogels in biomedical applications.
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