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Structure of 578729-05-2
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tert-Butyl (R)-(1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)carbamate delivers a chiral boronate handle with enhanced stability and compatibility in Suzuki-Miyaura coupling. The bulky tert-butyl carbamate group ensures excellent bench stability and minimizes side reactions, while the tetramethyl-1,3,2-dioxaborolane moiety enables efficient cross-coupling under mild conditions. This reagent integrates seamlessly into complex molecule synthesis workflows.
tert-Butyl (R)-(1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)carbamate serves as a stable, bench-ready boron building block for Suzuki-Miyaura coupling reactions. Its chiral benzylic center and orthogonal protecting group allow selective functionalization in complex molecule synthesis. The Bpin group enables reliable cross-coupling under mild conditions, while the tert-butyl carbamate offers excellent stability and straightforward deprotection via acidolysis, facilitating efficient access to chiral biaryl intermediates.
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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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: