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Structure of 1218791-01-5
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2-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazole features a boronate ester group enabling efficient Suzuki-Miyaura coupling under mild conditions. The electron-rich thiazole core enhances reactivity, while the tetramethyl-substituted dioxaborolane moiety ensures stability and moisture tolerance. This bench-stable reagent integrates readily into complex heterocyclic scaffolds during medicinal chemistry campaigns.
2-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazole serves as a robust boronate building block for Suzuki-Miyaura cross-coupling reactions. The tetramethylboronate group enables efficient coupling with aryl, heteroaryl, and vinyl halides under mild conditions. Its stability in air and moisture facilitates handling and storage, while the thiazole core provides a versatile scaffold for constructing biologically relevant heterocycles. This reagent offers excellent functional group tolerance and reproducible yields in synthetic 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: