9,9-Dimethyl-9H-fluoren-2-yl-boronic acid CAS: 333432-28-3
Catalog Number | XD93456 |
Product Name | 9,9-Dimethyl-9H-fluoren-2-yl-boronic acid |
CAS | 333432-28-3 |
Molecular Formula | C15H15BO2 |
Molecular Weight | 238.09 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
9,9-Dimethyl-9H-fluoren-2-yl-boronic acid is a highly useful compound in the field of organic chemistry and materials science. It is a boronic acid derivative with a fluorene skeleton, making it a versatile building block for the synthesis of various organic molecules.One notable application of 9,9-Dimethyl-9H-fluoren-2-yl-boronic acid is its use in cross-coupling reactions, particularly the Suzuki-Miyaura coupling. This reaction involves the formation of carbon-carbon bonds between an aryl or vinyl halide and an organoborane, facilitated by a suitable catalyst. The boronic acid moiety in9,9-Dimethyl-9H-fluoren-2-yl-boronic acid acts as the organoborane component, allowing for the synthesis of complex organic structures. This method is widely used in pharmaceutical and materials science research, where the formation of carbon-carbon bonds is crucial for generating target molecules with desired properties.Moreover, 9,9-Dimethyl-9H-fluoren-2-yl-boronic acid has been utilized in the development of organic semiconductors. The fluorene backbone confers excellent thermal and photochemical stability to the resulting molecules, making them suitable for optoelectronic applications. By incorporating the boronic acid group, which has electron-withdrawing properties, the resulting compounds exhibit enhanced electronic properties, such as improved charge mobility and conductivity. These properties are highly desirable for applications in organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), and organic photovoltaic devices (OPVs).Furthermore, the boronic acid functionality in 9,9-Dimethyl-9H-fluoren-2-yl-boronic acid enables its application in supramolecular chemistry. Boronic acids have the unique ability to form reversible covalent bonds with diols, making them valuable tools in the design of dynamic molecular systems. This property has been exploited in the development of self-assembled monolayers, molecular sensors, and drug delivery systems. By incorporating the fluorene scaffold, the resulting supramolecular assemblies exhibit enhanced stability and versatility, offering new possibilities in the field of materials science.In summary, 9,9-Dimethyl-9H-fluoren-2-yl-boronic acid is a valuable compound in organic synthesis, materials science, and supramolecular chemistry. It serves as a versatile building block for the synthesis of complex organic molecules, facilitates the development of high-performance organic semiconductors, and enables the design of dynamic supramolecular systems. Its multifunctional nature makes it an important tool for researchers in various scientific fields.