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Structure of 942070-20-4
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This boronate ester features a sterically hindered tetramethyl-1,3,2-dioxaborolane ring paired with a 2,5-dimethylthiophene moiety, delivering enhanced stability and reactivity in Suzuki-Miyaura coupling. The electron-rich thiophene unit facilitates efficient cross-coupling under mild conditions, enabling rapid access to complex arylated architectures in synthetic and medicinal chemistry workflows.
2-(2,5-Dimethylthiophen-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. The thiophene core imparts enhanced electronic stability and compatibility with diverse reaction conditions, enabling efficient C–C bond formation under mild catalytic systems. Its tetramethyl-substituted dioxaborolane ring ensures high chemical stability, resistance to hydrolysis, and ease of purification, making it ideal for modular synthesis of functionalized heterocycles and complex scaffolds in medicinal chemistry and materials science applications.
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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-H312-H315-H319-H332-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: