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Structure of 1218790-88-5
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This boronate moiety integrates a hydroxymethyl group at the 4-position and a methyl substituent at the 3-position on a phenyl ring, delivering enhanced solubility and stability under standard conditions. The ortho-methyl group modulates electronic properties while enabling selective functionalization in cross-coupling reactions.
(4-(Hydroxymethyl)-3-methylphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. The pendant hydroxymethyl group offers orthogonal functionality for downstream derivatization, while the boronic acid moiety provides excellent bench stability and compatibility with diverse reaction conditions. Its defined regiochemistry and predictable reactivity make it ideal for targeted synthesis of functionalized aromatic scaffolds in 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: