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Structure of 1261666-42-5
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This bench-stable arylmethanol features a para-amino group flanked by a bromine atom, enabling direct coupling in Suzuki-Miyaura and Buchwald-Hartwig reactions. The hydroxymethyl functionality supports derivatization into aldehydes or carboxylic acids, while the electron-rich aromatic core enhances reactivity in cross-coupling processes.
(3-Amino-4-bromophenyl)methanol serves as a versatile building block for pharmaceutical and agrochemical synthesis, enabling direct functionalization at the aromatic ring and side chain. Its amino and bromo groups offer orthogonal reactivity—facilitating Suzuki-Miyaura coupling, Buchwald-Hartwig amination, or electrophilic substitution—while the benzylic alcohol supports oxidation or protection strategies. The compound exhibits good bench stability and is amenable to purification via standard chromatography or crystallization, making it suitable for scalable intermediate development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: