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Structure of 103935-47-3
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2-Bromoethyl trifluoromethanesulfonate is a highly reactive alkylating agent featuring a triflate leaving group and a bromoethyl handle. This combination enables efficient C–C bond formation in synthetic organic chemistry, particularly in nucleophilic substitution reactions under mild conditions. The molecule's bench-stable nature supports reliable handling in process development workflows.
2-Bromoethyl trifluoromethanesulfonate serves as a versatile bifunctional electrophile, enabling efficient ring closure to form ethylene oxide derivatives under mild conditions. Its triflate group provides excellent leaving-group ability, facilitating nucleophilic substitution with amines, thiols, and carbanions. The molecule exhibits good bench stability and compatibility with diverse functional groups, making it a practical choice for constructing heterocyclic scaffolds and incorporating ether linkages in complex synthetic sequences.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 2927
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Class : 6.1 (8)
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Packing Group : Ⅱ
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Hazard Statements : H301+H311+H331-H314
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P330+P331-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P330-P361+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: