Chemical Name: | [2-[tert-butyl(dimethyl)silyl]oxyphenyl]boronic acid |
CAS Number: | 929277-63-4 |
Product Number: | AG00IHE5(AGN-PC-01MCRI) |
Synonyms: | |
MDL No: | |
Molecular Formula: | C12H21BO3Si |
Molecular Weight: | 252.1898 |
The (2-((tert-Butyldimethylsilyl)oxy)phenyl)boronic acid is a versatile compound widely used in chemical synthesis for its unique properties. It serves as a crucial building block in organic reactions, particularly in the field of modern organic synthesis. Due to its boronic acid functionality, this compound has found applications in Suzuki-Miyaura cross-coupling reactions for the formation of carbon-carbon bonds. Moreover, its tert-butyldimethylsilyl (TBS) protecting group enhances the compound's stability and reactivity, making it an excellent choice in the synthesis of complex organic molecules. In addition, the presence of the TBS group enables selective deprotection under mild conditions, offering control over the reaction process. Researchers and chemists rely on the (2-((tert-Butyldimethylsilyl)oxy)phenyl)boronic acid for its role in streamlining synthetic pathways and enabling the efficient construction of various organic compounds with high precision and yield.