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Structure of 20201-03-0
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2-Chloro-4-nitrobenzene-1-sulfonyl chloride features a reactive sulfonyl chloride group flanked by electron-withdrawing chlorine and nitro substituents, enabling efficient coupling in synthetic transformations. This bench-stable reagent integrates readily into aromatic sulfonamide architectures under mild conditions, offering high functional group tolerance and predictable regiochemistry for advanced organic synthesis.
2-Chloro-4-nitrobenzene-1-sulfonyl chloride serves as a versatile sulfonylating agent in synthetic organic chemistry, enabling efficient introduction of sulfonamide functionalities under mild conditions. Its reactivity is enhanced by the electron-withdrawing nitro group and the labile chloride, facilitating nucleophilic substitution with amines and alcohols. The compound exhibits good bench stability and compatibility with diverse functional groups, making it well-suited for the construction of sulfonamide-based building blocks in medicinal chemistry and agrochemical research.
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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#: 2928
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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: