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Structure of 859833-13-9
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This boronate-functional thiazole integrates seamlessly into Suzuki-Miyaura cross-coupling reactions under standard conditions. The tetramethyl-1,3,2-dioxaborolane moiety provides enhanced stability and moisture tolerance, while the 2,4-dimethyl substitution pattern minimizes undesired side reactions. This bench-stable reagent enables efficient access to complex heterocyclic architectures in medicinal chemistry and materials science.
2,4-Dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazole serves as a versatile boron-containing building block for palladium-catalyzed cross-coupling reactions. The thiazole core exhibits excellent bench stability and tolerates a range of functional groups, enabling efficient construction of biologically relevant heterocyclic scaffolds. Its steric and electronic profile facilitates reliable coupling with aryl and vinyl halides, making it well-suited for medicinal chemistry and materials synthesis 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: