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Structure of 1326714-48-0
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7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]thiazole features a boronate ester group conjugated to a benzo[d]thiazole core, enabling efficient Suzuki-Miyaura cross-coupling reactions. The tetramethyl-substituted dioxaborolane moiety enhances stability and shelf life under ambient conditions. This bench-stable reagent integrates readily into complex molecular architectures, particularly in the synthesis of biaryl systems for pharmaceutical and materials applications.
7-(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. The boryl group enables efficient C–C bond formation under mild conditions, with excellent functional group tolerance and bench stability. This reagent functions effectively in the synthesis of biaryl scaffolds common in pharmaceutical and materials chemistry, offering high reproducibility and ease of purification in standard reaction workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: