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Structure of 20712-12-3
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This bench-stable arylmethanol features a brominated aromatic ring and a primary alcohol group, enabling direct incorporation into cross-coupling reactions. The para-positioned amino substituent enhances reactivity in Suzuki-Miyaura processes, while the hydroxyl moiety offers a handle for derivatization.
(2-Amino-5-bromophenyl)methanol serves as a versatile building block for the synthesis of brominated aniline derivatives and heterocyclic scaffolds. Its amino and hydroxymethyl groups enable sequential functionalization, with the amine facilitating electrophilic substitution and the alcohol supporting orthogonal protection or coupling reactions. The compound exhibits good bench stability and is compatible with standard purification techniques, making it well-suited for medicinal chemistry campaigns and process development workflows.
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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: