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Structure of 27006-02-6
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This boronate moiety integrates a sterically hindered aryl scaffold with dual methyl groups flanking a bromo substituent, enabling selective cross-coupling under standard conditions. The hydroxymethyl functionality provides a handle for downstream derivatization and enhances solubility in polar solvents.
(4-Bromo-3,5-dimethylphenyl)methanol serves as a versatile building block in medicinal chemistry and materials synthesis, offering a brominated aryl methyl alcohol functionality. Its bench-stable nature and tolerance to common reaction conditions enable straightforward derivatization via nucleophilic substitution or coupling reactions. The ortho-methyl groups provide steric protection and enhance metabolic stability, making it suitable for constructing complex heterocyclic scaffolds and functionalized aromatic 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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: