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Structure of 635305-45-2
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This boronate ester features a chloro-substituted methoxyaryl group, enabling efficient coupling in Suzuki-Miyaura reactions. The tetramethyl-dioxaborolane scaffold ensures high stability and ease of handling under standard conditions.
2-(5-Chloro-2-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron building block for palladium-catalyzed cross-coupling reactions. Its ortho-chloro and methoxy substituents enable selective functionalization in Suzuki-Miyaura couplings, facilitating efficient access to biaryl scaffolds common in pharmaceutical intermediates. The tetramethyl-substituted dioxaborolane core ensures high reactivity and resistance to protodeboronation, while the robustness simplifies handling and purification in routine 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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: