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Structure of 302577-73-7
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Ethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate delivers a stable, moisture-tolerant boronate ester handle for cross-coupling reactions. The tetramethyl-substituted dioxaborolane enhances shelf life and reactivity under standard conditions. This compound integrates seamlessly into Suzuki-Miyaura protocols, enabling efficient C–C bond formation with aryl and vinyl halides.
Ethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. Its tetramethyl-substituted dioxaborolane moiety ensures excellent shelf stability and functional group tolerance, enabling efficient C–C bond formation under mild conditions. The ethyl ester group provides a handle for subsequent transformations, facilitating access to diverse alkylated aromatic and heteroaromatic scaffolds in medicinal chemistry and materials synthesis 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: