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*For research and further manufacturing use only, not for direct human use.
Structure of 62932-94-9
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This bromoketone features a phenolic hydroxyl and pendant hydroxymethyl group, enabling direct functionalization in late-stage synthesis. The electrophilic bromine facilitates nucleophilic substitution, while the ketone serves as a handle for reductive or condensation chemistry. Bench-stable under standard conditions, it supports efficient derivatization in medicinal chemistry workflows.
2-Bromo-1-[4-hydroxy-3-(hydroxymethyl)phenyl]ethan-1-one serves as a versatile building block for the synthesis of bioactive phenolic scaffolds. The molecule combines a bromoacetophenone motif with orthogonal hydroxyl and hydroxymethyl groups, enabling selective derivatization via Suzuki-Miyaura coupling, etherification, or oxidation. Its bench-stable nature and compatibility with standard purification methods make it well-suited for medicinal chemistry campaigns targeting kinase inhibitors and anti-inflammatory agents.
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: