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Structure of 52221-92-8
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This bench-stable bromophenylpropanol features a reactive bromide handle and primary alcohol functionality, enabling direct coupling in cross-coupling reactions or derivatization. The para-brominated aromatic ring supports palladium-mediated transformations, while the aliphatic chain provides synthetic flexibility for building complex architectures in medicinal chemistry and materials science.
3-(2-Bromo-phenyl)-propan-1-ol serves as a versatile building block for the synthesis of biologically active molecules and pharmaceutical intermediates. Its benzylic bromide functionality enables efficient nucleophilic substitution, while the primary alcohol supports oxidation, protection, or coupling reactions. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for multi-step synthetic sequences in medicinal chemistry and process development.
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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: