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Structure of 1029438-23-0
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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzenethiol integrates a boronate ester with a thiol group, enabling efficient Suzuki-Miyaura coupling and site-specific conjugation. The tetramethyl-substituted dioxaborolane enhances stability and reactivity under standard conditions. This bifunctional scaffold supports modular synthesis in medicinal chemistry and materials science.
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzenethiol serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. The thiol group enables orthogonal functionalization and facilitates conjugation in bioconjugate chemistry, while the tetramethylboronate moiety ensures high reactivity under mild conditions. Its robustness, ease of purification, and compatibility with diverse reaction partners make it a practical choice for constructing aryl-thioether linkages in medicinal chemistry and materials synthesis.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301+H311+H331-H315-H319
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361+P364-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: