• 1. Examination of the hydrogen-bonding networks in small water clusters (n = 2–5, 13, 17) using absolutely localized molecular orbital energy decomposition analysis?
  Erika A. Cobar,Paul R. Horn,Robert G. Bergman,Martin Head-Gordon Phys. Chem. Chem. Phys., 2012,14, 15328-15339
• 2. Excellent humidity sensor based on ultrathin HKUST-1 nanosheets?
  Qiaoe Wang,Meiling Lian,Xiaowen Zhu,Xu Chen RSC Adv., 2021,11, 192-197
• 3. Excellent energy storage performance in NaNbO3-based relaxor antiferroeic ceramics under a low electric field
  XuxinCheng,XiaomingChen,PengyuanFan
• 4. Exchanged ligands on the surface of a giant cluster: [(MoO3)176(H2O)63(CH3OH)17Hn](32 – n)–
  Chem. Commun., 1998, 1501-1502
• 5. Estimates of hydride ion stability in condensed systems: energy of formation and solvation in aqueous and polar-organic solvents
  Craig A. Kelly,David R. Rosseinsky Phys. Chem. Chem. Phys., 2001,3, 2086-2090

3,3'-(Ethane-1,2-diylbis(oxy))bis(3,1-phenylene)diboronic Acid Pinacol Ester (CAS No. 1073353-94-2): A Versatile Boronic Acid Derivative for Advanced Applications

3,3'-(Ethane-1,2-diylbis(oxy))bis(3,1-phenylene)diboronic Acid Pinacol Ester (CAS No. 1073353-94-2) is a highly specialized boronic acid derivative that has garnered significant attention in the fields of organic synthesis, materials science, and pharmaceutical research. This compound, characterized by its unique diboronic acid pinacol ester structure, serves as a critical building block for the development of advanced materials and bioactive molecules. Its ability to participate in Suzuki-Miyaura cross-coupling reactions makes it indispensable in the synthesis of complex organic frameworks.

The molecular structure of 3,3'-(Ethane-1,2-diylbis(oxy))bis(3,1-phenylene)diboronic Acid Pinacol Ester features two boronic acid pinacol ester groups linked by an ethane-1,2-diylbis(oxy) bridge. This configuration enhances its stability and reactivity, making it a preferred choice for researchers working on covalent organic frameworks (COFs) and metal-organic frameworks (MOFs). These materials are at the forefront of innovations in gas storage, catalysis, and drug delivery systems, aligning with the growing demand for sustainable and efficient technologies.

In the pharmaceutical industry, 3,3'-(Ethane-1,2-diylbis(oxy))bis(3,1-phenylene)diboronic Acid Pinacol Ester is valued for its role in the synthesis of boron-containing drugs. Boron-based compounds have shown promise in treating various diseases, including cancer and bacterial infections, due to their unique interaction with biological targets. The compound's pinacol ester groups protect the boronic acid functionality, ensuring stability during synthetic processes while allowing for controlled release in biological environments.

Recent advancements in green chemistry have further highlighted the importance of 3,3'-(Ethane-1,2-diylbis(oxy))bis(3,1-phenylene)diboronic Acid Pinacol Ester. Researchers are exploring its use in catalytic systems that minimize waste and reduce energy consumption. This aligns with global trends toward sustainable manufacturing practices and the development of eco-friendly materials. The compound's versatility and efficiency make it a key player in the transition to greener chemical processes.

The market for boronic acid derivatives is expanding rapidly, driven by their applications in organic electronics and photovoltaic materials. 3,3'-(Ethane-1,2-diylbis(oxy))bis(3,1-phenylene)diboronic Acid Pinacol Ester is particularly relevant in the development of organic light-emitting diodes (OLEDs) and solar cells, where its ability to form stable conjugated systems is highly advantageous. As the demand for renewable energy solutions grows, this compound is poised to play a pivotal role in next-generation technologies.

For researchers and industry professionals, understanding the properties and applications of 3,3'-(Ethane-1,2-diylbis(oxy))bis(3,1-phenylene)diboronic Acid Pinacol Ester is essential. Its compatibility with various synthetic methodologies, combined with its stability and reactivity, makes it a valuable tool in the design of innovative materials and therapeutics. As scientific exploration continues to uncover new possibilities, this compound is expected to remain at the forefront of chemical innovation.

In summary, 3,3'-(Ethane-1,2-diylbis(oxy))bis(3,1-phenylene)diboronic Acid Pinacol Ester (CAS No. 1073353-94-2) is a multifaceted compound with broad applications in cutting-edge research and industrial processes. Its unique structural features and functional versatility make it indispensable in fields ranging from drug discovery to renewable energy. As the scientific community continues to explore its potential, this compound is set to drive significant advancements in chemistry and materials science.

• 925916-59-2(4,4,5,5-tetramethyl-2-3-(propan-2-yloxy)phenyl-1,3,2-dioxaborolane)
• 959972-40-8(2-4-(2-methoxyethoxy)phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane)
• 957061-07-3(1,2-Di(4-boronophenoxy)ethane, dipinacol ester)
• 517874-21-4(2-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane)
• 664991-83-7(4-(Oxiran-2-ylmethoxy)phenylboronic Acid, pinacol ester)
• 1147105-68-7(4-Ethoxyphenylboronic Acid Pinacol Ester)
• 1235566-06-9(3-ethoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol)
• 1005010-05-8(2-3-Methoxy-4-(2-methoxyethoxy)phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane)
• 741699-47-8(2-4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxyethan-1-ol)
• 1338916-31-6(2-(3- Isobutoxyphenyl)-4,4,5,5-tetramethyl-1.3.2-dioxaborolane)