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Structure of 713-21-3
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2-Fluoro-5-nitrobenzenesulfonyl chloride features a sulfonyl chloride group flanked by electron-withdrawing fluorine and nitro substituents, enhancing reactivity in nucleophilic aromatic substitution. This bench-stable reagent facilitates efficient sulfonamide formation under mild conditions, offering high selectivity for functionalization in complex molecular architectures.
2-Fluoro-5-nitrobenzenesulfonyl chloride serves as a versatile sulfonylating agent for the selective introduction of sulfonamide groups under mild conditions. Its electron-withdrawing fluorine and nitro substituents enhance reactivity while maintaining bench stability, enabling efficient functionalization of amines, including sensitive heterocyclic and peptide substrates. The compound facilitates clean, high-yielding transformations with minimal side reactions, supporting scalable synthesis workflows in medicinal chemistry and agrochemical development.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3265
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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-P280-P301+P330+P331-P304+P340
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Lot numbers can be found on the outside label of a product: