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Structure of 886593-45-9
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This boronate moiety integrates a sterically shielded hydroxyl group, enhancing stability under standard conditions. The para-hydroxyisopropyl substitution pattern supports efficient coupling in Suzuki-Miyaura reactions while minimizing protodeboronation. Ideal for constructing complex biaryl architectures in medicinal chemistry and materials synthesis.
(4-(2-Hydroxypropan-2-yl)phenyl)boronic acid serves as a stable, bench-ready arylboronic acid that facilitates Suzuki-Miyaura cross-coupling reactions with high functional group tolerance. Its tertiary alcohol-containing substituent enhances solubility and reduces oxidation susceptibility, enabling reliable coupling in diverse reaction conditions. This derivative functions effectively in the synthesis of biaryl scaffolds for medicinal chemistry and materials science applications.
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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: