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Structure of 859169-20-3
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This boronate ester features a para-ethoxycarbonylmethyl substituent that enhances solubility and stability under standard conditions. The pinacol protection group enables reliable handling and compatibility with diverse cross-coupling reactions, facilitating efficient incorporation into complex molecular architectures.
4-Ethoxycarbonylmethylphenylboronic acid pinacol ester serves as a stable, bench-friendly building block for Suzuki-Miyaura coupling reactions. Its pinacol boronate ester functionality enhances air and moisture stability while enabling efficient C–C bond formation under standard catalytic conditions. The ethoxycarbonylmethyl group provides a versatile handle for further functionalization, including hydrolysis to the corresponding carboxylic acid or derivatization in multi-step synthesis. Functions reliably in the construction of biaryl scaffolds and complex heterocycles relevant to 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: