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Structure of 2135443-14-8
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rel-Ethyl (1R,2S)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopropane-1-carboxylate features a stereodefined cyclopropylboronate moiety that integrates readily into cross-coupling reactions. This bench-stable reagent enables efficient C–C bond formation under mild conditions, delivering structural diversity in complex molecule synthesis.
rel-Ethyl (1R,2S)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopropane-1-carboxylate serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. Its cyclopropyl motif imparts rigidity and defined stereochemistry, enabling efficient construction of complex cyclic scaffolds. The tetramethylboronate group offers excellent functional group tolerance, low toxicity, and compatibility with diverse reaction conditions, facilitating rapid access to biologically relevant architectures in medicinal chemistry and process development 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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: