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Structure of 1614233-69-0
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This boronate ester features a 2,6-difluoro-3,5-dimethoxyphenyl moiety integrated into a tetramethyl-substituted dioxaborolane framework. The electron-rich aryl group enhances reactivity in Suzuki-Miyaura couplings, while the sterically shielded boron center ensures stability under ambient conditions and tolerance to moisture.
2-(2,6-Difluoro-3,5-dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. The difluorodimethoxyaryl moiety enables selective functionalization in complex molecule synthesis, with the tetramethyl-substituted dioxaborolane enhancing stability and facilitating purification. Its compatibility with diverse reaction conditions makes it a practical reagent for constructing biaryl 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-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: