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Structure of 331958-92-0
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This boronate ester features a conjugated butenyl substituent that enhances reactivity in cross-coupling processes. The tetramethyl-substituted dioxaborolane ring ensures high stability and low hydrolysis rates, while phenothiazine stabilization prevents decomposition during storage and handling under ambient conditions.
2-(But-3-en-1-yl)-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 tetramethyl-substituted dioxaborolane moiety enhances air and moisture stability, while the terminal alkene functionality enables direct incorporation into complex molecular architectures. Its compatibility with diverse reaction conditions and ease of purification make it ideal for iterative synthesis workflows in medicinal chemistry and materials science.
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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 : H227-H302
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Precautionary Statements : P210-P264-P270-P280-P330-P370+P378-P403-P501
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Lot numbers can be found on the outside label of a product: