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Structure of 2425-28-7
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2-Bromo-1-phenylethan-1-ol features a chiral benzylic center bearing both bromine and hydroxyl groups, enabling direct functionalization in asymmetric synthesis. This bench-stable reagent integrates readily into C–C bond-forming sequences and serves as a precursor for enantioselective transformations.
2-Bromo-1-phenylethan-1-ol serves as a versatile building block in synthetic organic chemistry, enabling efficient access to phenethyl derivatives via substitution and elimination reactions. Its bromide functionality facilitates nucleophilic displacement under mild conditions, while the benzylic alcohol offers compatibility with oxidation, protection, and coupling protocols. The compound exhibits good bench stability and is readily purified by distillation or chromatography, supporting its use in iterative synthesis and scale-up applications.
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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: