(4-Bromo-3,5-dimethylthiophen-2-yl)boronicacid
98%
science Other reagents with same CAS 172872-73-0
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid group enables efficient carbon-carbon bond formation with aryl or heteroaryl halides, facilitating the construction of biaryl structures. The bromo and methyl substituents on the thiophene ring enhance reactivity and influence electronic properties, making it valuable in the development of functional materials, such as organic semiconductors and conjugated polymers. Commonly employed in medicinal chemistry for building blocks in drug discovery due to the stability and modularity it offers in synthetic pathways.
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