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Structure of 247129-85-7
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This sulfonium salt delivers a reactive bromoethyl handle for efficient functionalization in synthetic organic chemistry. The diphenylsulfonium moiety enhances stability and solubility, while the trifluoromethanesulfonate counterion enables rapid displacement under mild conditions. Ideal for C–C and C–heteroatom bond formation in complex molecule synthesis.
(2-Bromoethyl)diphenylsulfonium trifluoromethanesulfonate serves as a highly effective alkylating agent for nucleophilic substitution reactions, enabling efficient introduction of the 2-bromoethyl group under mild conditions. Its bench-stable nature and compatibility with diverse functional groups make it ideal for synthesizing sulfonium salts, bioactive molecules, and heterocyclic scaffolds in medicinal chemistry workflows.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: