Sulfonyl Halides

Sulfonyl Halides

Sulfonyl halides are highly reactive electrophilic reagents widely used in sulfonamide synthesis, peptide coupling, polymer modification, and functional-material construction. Their strong electron-withdrawing sulfonyl group activates the halide for nucleophilic substitution, enabling formation of sulfones, sulfonates, sulfonylureas, and sulfur-containing heterocycles. Sulfonyl chlorides such as tosyl chloride and mesyl chloride are indispensable in protecting-group chemistry and activation of alcohols. In pharmaceuticals, sulfonyl halides provide key intermediates for antibiotics, antihypertensives, and antidiabetic agents. Their high reactivity and broad functional compatibility make sulfonyl halides essential tools in synthetic and industrial chemistry.

3-Acetylbenzenesulfonyl Fluoride CAS NO 709-60-4

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CAS No.:709-60-4

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Content:99.90%

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2-Fluoro-5-Nitrobenzenesulfonyl Chloride CAS NO 713-21-3

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CAS No.:713-21-3

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Ethanesulfonic Acid Fluoride CAS NO 754-03-0

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CAS No.:754-03-0

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2-(1H-1,2,3-Benzotriazol-1-Yl)Ethanesulfonyl Fluoride CAS NO 71517-82-3

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CAS No.:71517-82-3

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2-Fluoroethanesulfonyl Chloride CAS NO 762-68-5

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CAS No.:762-68-5

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Propanesulphonyl Fluoride CAS NO 762-69-6

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CAS No.:762-69-6

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2,2,2-Trichloroethyl Chlorosulfate CAS NO 764-09-0

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CAS No.:764-09-0

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Benzenesulfonyl Chloride, 2-Chloro-5-(Trifluoromethoxy)- CAS NO 77797-65-0

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CAS No.:77797-65-0

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