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Structure of 4254-67-5
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This bromoketone features a benzyloxy-substituted phenyl ring paired with a reactive α-bromo acetyl group. The electron-rich aromatic system enhances conjugation, while the bromoacetyl moiety enables nucleophilic displacement reactions. Designed for synthetic integration in pharmaceutical intermediates and functionalized building blocks, it offers high reactivity under mild conditions.
1-(4-(Benzyloxy)phenyl)-2-bromoethanone serves as a versatile synthetic intermediate for constructing aryl-alkyl ketone motifs and functionalized benzodioxole scaffolds. Its bromoacetyl group enables efficient nucleophilic substitution, Michael addition, and coupling reactions under mild conditions. The benzyloxy substituent provides orthogonal protection and enhances solubility, facilitating purification and downstream transformations in medicinal chemistry workflows.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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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 : Ⅱ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P270-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: