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Structure of 17102-63-5
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This boronate moiety integrates a bromo-substituted methoxyphenyl group with a primary alcohol, enabling direct functionalization in cross-coupling reactions. The para-bromo and ortho-methoxy pattern enhances reactivity while maintaining bench-stable handling under standard conditions.
(4-Bromo-2-methoxyphenyl)methanol serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the benzylic position. Its bromo group facilitates palladium-catalyzed cross-coupling reactions, while the methoxy substituent provides moderate electron-donating character and ortho-directing effects. The benzylic alcohol functionality offers a handle for oxidation, protection, or derivatization, supporting diverse synthetic routes. Bench-stable and readily purified by flash chromatography, it functions effectively in multi-step syntheses of bioactive heterocycles 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
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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: