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Structure of 943911-67-9
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N-Ethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide features a boronate ester group that enables efficient Suzuki-Miyaura cross-coupling reactions. The tetramethyl-substituted dioxaborolane moiety enhances stability and shelf life under ambient conditions. This bench-stable reagent integrates readily into synthetic sequences for constructing biaryl scaffolds in medicinal chemistry and materials science applications.
N-Ethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide serves as a versatile boronate building block in Suzuki-Miyaura cross-coupling reactions. Its stable boronate ester group enables efficient C–C bond formation under mild conditions, with excellent functional group tolerance and bench stability. The N-ethyl amide moiety enhances solubility and modulates reactivity, facilitating integration into complex molecular architectures. This compound functions reliably in the synthesis of biaryl scaffolds and pharmaceutical 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 : H317-H319
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Precautionary Statements : P261-P264-P272-P280-P302+P352-P362+P364-P501
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Lot numbers can be found on the outside label of a product: