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Structure of 220556-03-6
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4-(2-Bromoethyl)benzene-1,2-diol features a phenolic diol scaffold flanked by a bromoethyl side chain, enabling direct functionalization via nucleophilic substitution. This bifunctional architecture supports conjugation workflows in synthetic organic chemistry and medicinal discovery, where the reactive bromide facilitates site-specific derivatization under mild conditions.
4-(2-Bromoethyl)benzene-1,2-diol serves as a versatile diol-containing building block for the synthesis of functionalized aromatic scaffolds. The pendant bromoethyl group enables efficient post-functionalization via nucleophilic substitution, while the ortho-diol moiety offers opportunities for selective protection or metal-catalyzed coupling. Bench-stable and compatible with standard purification techniques, it facilitates the construction of complex heterocycles and bioactive intermediates in medicinal chemistry workflows.
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GHS Pictogram :
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GHS No : GHS06,GHS08
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331-H341
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: