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Structure of 51527-73-2
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2,4,6-Trichlorobenzene-1-sulfonyl chloride features a highly electrophilic sulfonyl chloride group flanked by three chlorine substituents, enabling efficient coupling reactions in synthetic organic chemistry. This electron-deficient aryl scaffold facilitates rapid functionalization under mild conditions, delivering robust sulfonamide and sulfonate derivatives with excellent regiocontrol. The molecule exhibits enhanced stability compared to less substituted analogs, simplifying handling and storage.
2,4,6-Trichlorobenzene-1-sulfonyl chloride serves as a highly reactive sulfonylating agent for the efficient introduction of the trichlorobenzene-1-sulfonyl group into diverse substrates. Its strong electrophilicity facilitates rapid reaction with nucleophiles such as amines and alcohols under mild conditions, enabling straightforward synthesis of sulfonamide and sulfonate derivatives. The electron-withdrawing trichloro substituents enhance reactivity while maintaining bench stability, making it a practical choice for functional group interconversions in synthetic organic chemistry and API intermediate 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 : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: