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Structure of 1314306-11-0
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This boronate ester features a sterically protected tetramethyl-1,3,2-dioxaborolane group attached to a thiazole core bearing two methyl substituents. The electron-deficient thiazole ring enables efficient cross-coupling reactions under mild conditions. This bench-stable reagent integrates readily into Suzuki-Miyaura coupling workflows for constructing complex heterocyclic architectures with high functional group tolerance.
2,5-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazole serves as a stable, bench-ready boronate building block for palladium-catalyzed cross-coupling reactions. The tetramethylboronate moiety enables efficient Suzuki-Miyaura coupling under mild conditions, while the electron-rich thiazole core provides structural rigidity and functional group tolerance. This compound facilitates rapid assembly of substituted thiazole scaffolds in medicinal chemistry and materials synthesis.
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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: