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Structure of 929626-16-4
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This boronate reagent features a chloro-methoxy-substituted aryl group enabling efficient cross-coupling in Suzuki-Miyaura reactions. The tetramethyl-dioxaborolane scaffold ensures excellent stability, solubility in common organic solvents, and compatibility with air- and moisture-tolerant protocols.
2-(3-Chloro-5-methoxyphenyl)-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 3-chloro-5-methoxyphenyl moiety enables selective functionalization under standard catalytic conditions, with the tetramethyl-substituted dioxaborolane ring providing enhanced stability and ease of purification. Its compatibility with diverse reaction partners makes it a practical choice for constructing complex aryl architectures in medicinal chemistry and materials synthesis.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P405-P501
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Lot numbers can be found on the outside label of a product: