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Structure of 4025-67-6
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4-Hydroxybenzenesulfonyl chloride features a phenolic hydroxyl group adjacent to a sulfonyl chloride moiety, enabling selective derivatization in aqueous or mixed solvents. This bifunctional reagent facilitates the synthesis of sulfonamide-linked biologics and bioconjugates under mild conditions. The electron-withdrawing sulfonyl chloride activates the aromatic ring for nucleophilic substitution, while the hydroxyl group provides hydrogen-bonding capacity and enhanced solubility.
4-Hydroxybenzenesulfonyl chloride serves as a versatile sulfonating agent and synthetic intermediate, enabling direct introduction of the 4-hydroxybenzenesulfonyl group into nucleophilic substrates. Its reactivity facilitates efficient derivatization of amines, alcohols, and thiols under mild conditions, with the phenolic hydroxyl group offering subsequent functionalization potential. The compound exhibits good bench stability and enables straightforward purification, making it well-suited for use in medicinal chemistry and API scaffold 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#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H290-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: