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Structure of 213211-69-9
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2-Ethoxyphenylboronic acid features a boronate moiety attached to an electron-rich phenyl ring, enabling efficient Suzuki-Miyaura cross-coupling reactions. The ethoxy substituent enhances solubility in polar organic solvents and contributes to improved stability under standard handling conditions. This compound serves as a reliable building block for synthesizing functionalized biaryls and complex pharmaceutical intermediates.
2-Ethoxyphenylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its ortho-ethoxy substitution enhances solubility and stability compared to unsubstituted analogs, while the boronic acid group exhibits predictable reactivity with aryl halides and triflates. The compound demonstrates good bench stability, facilitates straightforward purification, and functions reliably in the synthesis of biaryl scaffolds relevant to pharmaceutical and materials chemistry.
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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: