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Structure of 1225053-32-6
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This boronate-functionalized thiazole integrates readily into Suzuki-Miyaura coupling reactions under standard conditions, delivering biaryl architectures with high efficiency. The tetramethyl-1,3,2-dioxaborolane moiety ensures excellent stability and moisture tolerance during handling.
2-Phenyl-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 moiety ensures excellent bench stability and compatibility with a wide range of reaction conditions. It facilitates efficient C–C bond formation with aryl, heteroaryl, and vinyl halides, enabling rapid access to biaryl and extended conjugated systems. Its functional group tolerance and ease of purification make it a practical choice for synthetic workflows in medicinal chemistry and materials science.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: