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Structure of 1002309-47-8
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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]thiazole features a boronate ester group attached to a benzothiazole scaffold, enabling efficient Suzuki-Miyaura cross-coupling reactions. The tetramethyl-substituted dioxaborolane moiety enhances stability and reactivity under standard conditions. This compound serves as a robust building block for constructing biaryl architectures in medicinal chemistry and materials science applications.
6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]thiazole serves as a robust boronate building block for Suzuki-Miyaura cross-coupling reactions. Its stability under ambient conditions and tolerance to diverse functional groups enable efficient construction of biaryl architectures. The dioxaborolane moiety facilitates mild reaction conditions and high yields, making it ideal for late-stage functionalization in medicinal chemistry and materials science applications.
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Lot numbers can be found on the outside label of a product: