4-Trifluoromethylphenylboronic acid, pinacol ester (CAS 214360-65-3)
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4-Trifluoromethylphenylboronic acid, pinacol ester functions as a key building block in organic synthesis. It acts as a versatile reagent in the formation of carbon-carbon and carbon-heteroatom bonds, making it important for the construction of complex molecular structures. Its mechanism of action involves participating in cross-coupling reactions, Suzuki-Miyaura coupling, and other transformations, enabling the creation of diverse chemical entities with potential applications in materials science,and agrochemicals. 4-Trifluoromethylphenylboronic Acid, Pinacol Ester′s ability to undergo selective and efficient reactions at the molecular level may be in the development of new compounds and materials with tailored properties. Its role in facilitating the synthesis of novel molecules contributes to the advancement of chemical applications and the exploration of new frontiers in molecular design and functional materials.
4-Trifluoromethylphenylboronic acid, pinacol ester (CAS 214360-65-3) References
- C-H functionalization logic enables synthesis of (+)-hongoquercin A and related compounds. | Rosen, BR., et al. 2013. Angew Chem Int Ed Engl. 52: 7317-20. PMID: 23740529
- Highly Efficient Deep-Blue Electroluminescence from a A−π–D−π–A Structure Based Fluoresence Material with Exciton Utilizing Efficiency above 25%IF 6.959Q1B3EI | Minna Hou, Hua Wang*, Yanqin Miao, Huixia Xu, Zhen Guo, Zhikuan Chen, Xiaoqing Liao, Lu Li, Jie Li, and Kunpeng Guo. 2018. ACS Appl. Energy Mater. 1: 3243–3254.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
4-Trifluoromethylphenylboronic acid, pinacol ester, 1 g | sc-311063 | 1 g | $71.00 | |||
4-Trifluoromethylphenylboronic acid, pinacol ester, 5 g | sc-311063A | 5 g | $153.00 |