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Structure of 1451391-54-0
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This boronic acid features a hydroxymethyl group adjacent to the boronate, enhancing solubility and stability. The para-methyl substitution provides electron-donating character, improving coupling efficiency in Suzuki-Miyaura reactions. Bench-stable under standard conditions, it integrates seamlessly into complex molecule synthesis workflows.
(3-(Hydroxymethyl)-4-methylphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. The ortho-hydroxymethyl and meta-methyl groups provide enhanced solubility and functional group tolerance, while the boronic acid moiety exhibits excellent bench stability and ease of purification—ideal for iterative synthesis of complex aromatic scaffolds and pharmaceutical intermediates.
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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: