Description

1,1,2,2-Tetrakis(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethene (CAS No. 1660996-72-4) is a highly specialized boronate ester compound with the molecular formula C₅₀H₆₄B₄O₈. This tetrafunctional boronic ester derivative features a central ethene core symmetrically substituted with four 4,4,5,5-tetramethyl-1,3,2-dioxaborolane groups, making it an exceptional building block for advanced materials synthesis. The compound’s unique structure offers exceptional stability and reactivity, particularly in Suzuki-Miyaura cross-coupling reactions and other transition metal-catalyzed processes. With a purity grade suitable for research and industrial applications, this product is ideal for developing luminescent materials, organic electronic components, and porous framework materials. The crystalline solid is supplied under inert conditions to ensure maximum shelf life and reactivity.

Properties

• CAS Number: 1660996-72-4
• Complexity: 1330
• IUPAC Name: 4,4,5,5-tetramethyl-2-[4-[1,2,2-tris[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]vinyl]phenyl]-1,3,2-dioxaborolane
• InChI: InChI=1S/C50H64B4O8/c1-43(2)44(3,4)56-51(55-43)37-25-17-33(18-26-37)41(34-19-27-38(28-20-34)52-57-45(5,6)46(7,8)58-52)42(35-21-29-39(30-22-35)53-59-47(9,10)48(11,12)60-53)36-23-31-40(32-24-36)54-61-49(13,14)50(15,16)62-54/h17-32H,1-16H3
• InChI Key: IMKQIUDDYPXPIU-UHFFFAOYSA-N
• Exact Mass: 836.4973397
• Molecular Formula: C50H64B4O8
• Molecular Weight: 836.3
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC=C(C=C2)C(=C(C3=CC=C(C=C3)B4OC(C(O4)(C)C)(C)C)C5=CC=C(C=C5)B6OC(C(O6)(C)C)(C)C)C7=CC=C(C=C7)B8OC(C(O8)(C)C)(C)C
• Topological: 73.8
• Monoisotopic Mass: 836.4973397
• Synonyms: 1,1,2,2-Tetrakis(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethene, 1660996-72-4, YSZC726, MFCD31700765, 4,4,5,5-tetramethyl-2-[4-[1,2,2-tris[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethenyl]phenyl]-1,3,2-dioxaborolane, AS-85909, CS-0110315, E74367, 2,2′,2”,2”’-(1,1,2,2-Ethenetetrayltetra-4,1-phenylene)tetrakis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)

Application

This tetrafunctional boronic ester is primarily employed as a key precursor in the synthesis of advanced organic electronic materials, particularly for constructing highly conjugated systems in OLED and OFET applications. Its multiple reactive sites enable the creation of complex polymeric networks for luminescent sensors and porous organic frameworks. Researchers also utilize this compound to develop novel aggregation-induced emission (AIE) materials for bioimaging applications.

If you are interested or have any questions, please contact us at support@atomfair.com

Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.