Description

2-Methyl-1,4-phenylene Bis(4-(((4-(acryloyloxy)butoxy)carbonyl)oxy)benzoate) (CAS No. 187585-64-4) is a high-purity, synthetic organic compound with the molecular formula C₃₇H₃₆O₁₄. This specialized chemical features a complex structure incorporating acryloyloxy and benzoate functional groups, making it highly reactive and suitable for advanced polymer and material science applications. Its IUPAC name, [3-methyl-4-[4-(4-prop-2-enoyloxybutoxycarbonyloxy)benzoyl]oxyphenyl] 4-(4-prop-2-enoyloxybutoxycarbonyloxy)benzoate, reflects its precise molecular architecture. Ideal for researchers and scientists, this compound is rigorously tested for consistency and purity, ensuring reliable performance in photopolymerization, liquid crystal displays (LCDs), and other high-tech material syntheses. Available in customizable quantities, it is packaged under strict quality control to meet laboratory and industrial standards.

Properties

• CAS Number: 187585-64-4
• Complexity: 1170
• IUPAC Name: [3-methyl-4-[4-(4-prop-2-enoyloxybutoxycarbonyloxy)benzoyl]oxy-phenyl] 4-(4-prop-2-enoyloxybutoxycarbonyloxy)benzoate
• InChI: InChI=1S/C37H36O14/c1-4-32(38)44-20-6-8-22-46-36(42)49-28-14-10-26(11-15-28)34(40)48-30-18-19-31(25(3)24-30)51-35(41)27-12-16-29(17-13-27)50-37(43)47-23-9-7-21-45-33(39)5-2/h4-5,10-19,24H,1-2,6-9,20-23H2,3H3
• InChI Key: ZKBUNGNDTCOGEU-UHFFFAOYSA-N
• Exact Mass: 704.21050582
• Molecular Formula: C37H36O14
• Molecular Weight: 704.7
• SMILES: CC1=C(C=CC(=C1)OC(=O)C2=CC=C(C=C2)OC(=O)OCCCCOC(=O)C=C)OC(=O)C3=CC=C(C=C3)OC(=O)OCCCCOC(=O)C=C
• Topological: 176
• Monoisotopic Mass: 704.21050582
• Synonyms: 2-methyl-1,4-phenylene bis(4-(((4-(acryloyloxy)butoxy)carbonyl)oxy)benzoate), 2-Methyl-1,4-phenylene Bis[4-[[[4-(acryloyloxy)butoxy]carbonyl]oxy]benzoate], 428-570-1, 187585-64-4, LC242, MFCD30179603, [3-methyl-4-[4-(4-prop-2-enoyloxybutoxycarbonyloxy)benzoyl]oxyphenyl] 4-(4-prop-2-enoyloxybutoxycarbonyloxy)benzoate, 4-[[[4-[(1-Oxo-2-propenyl)oxy]butoxy]carbonyl]oxy]benzoic acid 2-methyl-1,4-phenylene ester, bAcrBuOCaABzoMeP, ZKBUNGNDTCOGEU-UHFFFAOYSA-N, SCHEMBL453621, DTXSID001116343, BCP12367, C37H36O14, AKOS027460705, SB66931, 3-methyl-4-[4-({[4-(prop-2-enoyloxy)butoxy]carbonyl}oxy)benzoyloxy]phenyl 4-({[4-(prop-2-enoyloxy)butoxy]carbonyl}oxy)benzoate, DS-19158, LC-242;LC 242;Paliocolor LC 242, SY316575, DB-324027, CS-0158043, M3368, C73594, 2-methyl-1,4-phenylene bis(4-(((4-(acryloyloxy)butoxy) carbonyl)oxy)benzoate), 2-methyl-1,4-phenylenebis(4-(((4-(acryloyloxy)butoxy)carbonyl)oxy)benzoate), 1,1a(2)-(2-Methyl-1,4-phenylene) bis[4-[[[4-[(1-oxo-2-propen-1-yl)oxy]butoxy]carbonyl]oxy]benzoate], 2-Methyl-1,4-phenylene bis[4-[[[4-[(1-oxo-2-propen-1-yl)oxy]butoxy]carbonyl]oxy]-benzoate]

Application

This compound is primarily used in the development of advanced polymeric materials, particularly in photopolymerization processes for coatings, adhesives, and 3D printing resins. Its bifunctional acrylate groups make it a valuable crosslinking agent in liquid crystal displays (LCDs) to enhance optical properties and mechanical stability. Researchers also utilize it in the synthesis of high-performance liquid crystal polymers (LCPs) for electronics and aerospace applications.

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