Description

2-[[4-Bis[4-(2-prop-2-enoyloxyethoxycarbonylamino)phenoxy]phosphinothioyloxyphenyl]carbamoyloxy]ethyl prop-2-enoate (CAS: 1072454-85-3) is a high-purity, specialty chemical designed for advanced research and industrial applications. This compound features a complex molecular structure (C₃₆H₃₆N₃O₁₅PS) with reactive acrylate groups and a phosphinothioyl core, making it ideal for polymer chemistry, photo-crosslinking studies, and material science. Its precise synthesis ensures consistency for controlled experiments, while its unique thiophosphoryl and carbamate linkages offer tailored reactivity for custom modifications. Packaged under inert conditions to preserve stability, this product is suited for researchers requiring exacting standards in photoresists, adhesives, or functionalized polymers. Available in milligram to gram quantities with optional analytical certification.

Properties

• CAS Number: 1072454-85-3
• Complexity: 1230
• IUPAC Name: 2-[[4-bis[4-(2-prop-2-enoyloxyethoxycarbonylamino)phenoxy]phosphinothioyloxyphenyl]carbamoyloxy]ethyl prop-2-enoate
• InChI: InChI=1S/C36H36N3O15PS/c1-4-31(40)46-19-22-49-34(43)37-25-7-13-28(14-8-25)52-55(56,53-29-15-9-26(10-16-29)38-35(44)50-23-20-47-32(41)5-2)54-30-17-11-27(12-18-30)39-36(45)51-24-21-48-33(42)6-3/h4-18H,1-3,19-24H2,(H,37,43)(H,38,44)(H,39,45)
• InChI Key: KVTQWUZRSTYVOR-UHFFFAOYSA-N
• Exact Mass: 813.16047562
• Molecular Formula: C36H36N3O15PS
• Molecular Weight: 813.7
• SMILES: C=CC(=O)OCCOC(=O)NC1=CC=C(C=C1)OP(=S)(OC2=CC=C(C=C2)NC(=O)OCCOC(=O)C=C)OC3=CC=C(C=C3)NC(=O)OCCOC(=O)C=C
• Topological: 254
• Monoisotopic Mass: 813.16047562
• Synonyms: 1072454-85-3, SCHEMBL123934, KVTQWUZRSTYVOR-UHFFFAOYSA-N, DTXSID601112749, 1,1a(2),1a(2)a(2)-[Phosphinothioylidynetris(oxy-4,1-phenyleneiminocarbonyloxy-2,1-ethanediyl)] tri-2-propenoate, 2-Propenoic acid, 1,1′,1”-[phosphinothioylidynetris(oxy-4,1-phenyleneiminocarbonyloxy-2,1-ethanediyl)] ester

Application

This multifunctional acrylate derivative is primarily used in photopolymerization research, where its tri-branched structure enables crosslinked network formation under UV light. It serves as a key monomer in high-performance coatings, dental resins, or 3D printing photoresins due to its rapid curing and mechanical stability. The thiophosphoryl group may also facilitate flame-retardant applications in polymeric materials.

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