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1,3,4-Oxadiazole, 2,5-Bis[4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl]- CAS NO 1116122-85-0
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CAS No.:1116122-85-0
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
1,3,4-Oxadiazole, 2,5-Bis[4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl]- is a high-purity, functionalized organic building block featuring a central 1,3,4-oxadiazole core flanked by two pinacol boronate ester groups. This compound is specifically engineered for advanced cross-coupling reactions, serving as a critical precursor in the synthesis of complex organic electronic materials and pharmaceutical intermediates. It is essential for R&D chemists and process engineers in the organic electronics, pharmaceutical, and agrochemical sectors who require reliable, high-quality boron reagents for Suzuki-Miyaura and other palladium-catalyzed coupling protocols.
Application
- Suzuki-Miyaura Cross-Coupling Reactions: As a key monomer for constructing conjugated polymers and small molecules used in Organic Light-Emitting Diodes (OLEDs), Organic Photovoltaics (OPVs), and Field-Effect Transistors (OFETs).
- Pharmaceutical Intermediate Synthesis: For the precise construction of biaryl and heterobiaryl scaffolds found in active pharmaceutical ingredients (APIs) and drug candidates.
- Material Science Research: In the development of novel porous organic polymers (POPs), covalent organic frameworks (COFs), and other advanced functional materials.
- Agrochemical Development: As a building block for creating new compounds with potential herbicidal, fungicidal, or insecticidal activity.
- Ligand and Catalyst Design: For synthesizing complex chelating ligands or functionalized catalysts used in homogeneous catalysis.
- Chemical Biology Probes: In the synthesis of tagged molecules for studying biological processes and target engagement.
Basic Information
| Product Name | 1,3,4-Oxadiazole, 2,5-Bis[4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl]- |
| CAS No. | 1116122-85-0 |
| Molecular Formula | C28H36B2N2O6 |
| Molecular Weight | 518.22 g/mol |
| Synonyms | 2,5-Bis[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,4-oxadiazole; 2,5-Bis(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1,3,4-oxadiazole; 1,3,4-Oxadiazole-2,5-diylbis(4,1-phenylene)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane); BOD-2; B-2,5-Bis(4-boronopinacolate phenyl)-1,3,4-oxadiazole; 2,5-Di(4-boronopinacolatophenyl)-1,3,4-oxadiazole; 4,4'-(1,3,4-Oxadiazole-2,5-diyl)dibenzeneboronic acid bis(pinacol) ester |
| EINECS | Contact for details |
Quality Control
Every batch of our 1,3,4-Oxadiazole boronate ester is synthesized and purified under controlled conditions to ensure exceptional lot-to-lot consistency and reliability for sensitive cross-coupling applications. Our products undergo rigorous quality testing, including advanced chromatographic and spectroscopic methods, to ensure compliance with stringent internal specifications. Certificates of Analysis (COA) detailing purity, identity, and impurity profiles are available upon request to support your quality assurance and regulatory documentation needs.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This material is moisture-sensitive (hygroscopic) and should be handled under an inert atmosphere (e.g., nitrogen or argon) for long-term storage to maintain reactivity and purity. Keep away from strong oxidizers.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to structure |
| Purity (HPLC) | ≥ 97.0% |
| Water Content (KF) | ≤ 0.5% |
| Residue on Ignition | ≤ 0.1% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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