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Structure of 1246765-32-1
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This boronate ester features a methoxy-substituted aryl core paired with a methoxycarbonyl group, enhancing solubility and stability. The pinacol protection delivers bench-stable handling while enabling efficient Suzuki-Miyaura coupling under standard conditions. Ideal for constructing complex phenyl scaffolds in medicinal chemistry and materials synthesis.
2-Methoxy-4-methoxycarbonyl-phenyl-boronic acid pinacol ester serves as a stable, bench-ready building block for Suzuki-Miyaura cross-coupling reactions. Its ortho-methoxy and meta-methoxycarbonyl substituents provide enhanced solubility and functional group tolerance, enabling efficient C–C bond formation under mild conditions. The pinacol boronate ester resists protodeboronation and simplifies purification, making it ideal for constructing complex aryl scaffolds in medicinal chemistry and materials science 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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: