1. Basic Information and Parameters
2. Product Uses
3. How to Use
4. Usage Case Studies
5. Contact Information

Basic Information and Parameters

The product named "Factory Supply 9,9 - diphenyl - 9H - fluoreN - 2 - ylboronic acid" has the CAS number 400607 - 31 - 0. It is supplied directly from the factory, which often implies a competitive price and high - quality control. This boronic acid derivative with its specific molecular structure is an important compound in the field of organic synthesis. The purity of the product can usually be customized according to the customer's requirements, with common purity levels ranging from 95% to 99%. The appearance of the product is typically a white to off - white powder, which is relatively stable under normal storage conditions.

Product Uses

9,9 - diphenyl - 9H - fluoreN - 2 - ylboronic acid is widely used in organic synthesis and material science. In organic synthesis, it serves as a key intermediate for the construction of complex organic molecules through various coupling reactions, such as Suzuki - Miyaura coupling. This coupling reaction allows for the formation of carbon - carbon bonds, which is crucial for the synthesis of pharmaceuticals, agrochemicals, and advanced organic materials. In the field of material science, it can be incorporated into the structure of organic light - emitting diodes (OLEDs). The unique fluorescent properties of the fluorene moiety in the molecule can enhance the luminescence efficiency and color purity of OLEDs, making them suitable for high - performance display applications.

How to Use

When using 9,9 - diphenyl - 9H - fluoreN - 2 - ylboronic acid, it is important to follow proper laboratory procedures. First, ensure that the product is stored in a cool, dry place away from direct sunlight and oxidizing agents. Before use, carefully weigh the required amount of the product using a precise analytical balance. In a typical Suzuki - Miyaura coupling reaction, dissolve the boronic acid in an appropriate solvent, such as tetrahydrofuran (THF) or dimethylformamide (DMF). Then, add the appropriate palladium catalyst and base to the reaction mixture. The reaction is usually carried out under an inert atmosphere, such as nitrogen or argon, to prevent oxidation of the reactants. Monitor the reaction progress using thin - layer chromatography (TLC) or other analytical techniques. Once the reaction is complete, the product can be isolated and purified using standard purification methods, such as column chromatography or recrystallization.

Usage Case Studies

Case 1: Pharmaceutical Synthesis
A research group was working on the synthesis of a novel anti - cancer drug. They used 9,9 - diphenyl - 9H - fluoreN - 2 - ylboronic acid as a key building block in a Suzuki - Miyaura coupling reaction. By coupling the boronic acid with a suitable aryl halide, they were able to construct the core structure of the drug molecule. After further chemical modifications and purification steps, they obtained the final drug product with high purity and strong anti - cancer activity. The use of this boronic acid derivative significantly simplified the synthesis process and improved the overall yield of the drug.

Case 2: OLED Development
A company specializing in OLED technology incorporated 9,9 - diphenyl - 9H - fluoreN - 2 - ylboronic acid into the structure of their new OLED materials. By carefully designing the molecular structure and optimizing the synthesis process, they were able to improve the efficiency and stability of the OLEDs. The resulting OLED displays showed better color reproduction and longer lifespan, which helped the company gain a competitive edge in the market.

Contact Information

If you have any questions about our Factory Supply 9,9 - diphenyl - 9H - fluoreN - 2 - ylboronic acid, please feel free to contact us. Our email address is info@vivalr.com, and our phone number is (86) 15866781826. We are always ready to provide you with professional advice and high - quality products.