Benzenesulfonyl compounds
Benzenesulfonyl compounds are a class of organic compounds characterized by the presence of a benzenesulfonyl group, -SO?Ph (where Ph represents a phenyl group). These compounds find extensive application in various fields due to their unique reactivity and structural properties. They are often used as intermediates in the synthesis of pharmaceuticals, dyes, and agrochemicals. The presence of the sulfonyl group confers them with strong electrophilic properties, making them valuable reagents for substitution reactions such as sulfonamidation and amidation. Additionally, benzenesulfonyl compounds are known for their stabilizing effects on certain reactive intermediates, facilitating the control of reaction pathways in complex synthetic transformations. Their versatility and reactivity make them indispensable tools in organic chemistry research and industrial applications.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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4-(ethanesulfonyl)benzaldehyde | 50899-03-1 | C9H10O3S |
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Benzonitrile, 2-(phenylsulfonyl)- | 54737-49-4 | C13H9NO2S |
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Benzene, 1,4-dimethyl-2-(methylsulfonyl)- | 6462-29-9 | C9H12O2S |
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(E)-3-Cyclopentyl-2-(4-(methylsulfonyl)phenyl)prop-2-en-1-ol | 731017-34-8 | C15H20O3S |
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Benzene, 1-fluoro-4-[(1-methyl-2-propenyl)sulfonyl]- | 88576-31-2 | C10H11FO2S |
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1-benzyl-4-2-(4-chlorobenzenesulfonyl)ethylpiperazine | 883018-91-5 | C19H23ClN2O2S |
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1-Chloro-4-trifluoromethanesulfonylbenzene | 383-11-9 | C7H4ClF3O2S |
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1-Ethynyl-4-(methylsulfonyl)benzene | 340771-31-5 | C9H8O2S |
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2-aminobenzene-1-sulfonyl fluoride | 392-86-9 | C6H6FNO2S |
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Benzene,1-chloro-4-[1-chloro-2-(phenylsulfonyl)ethyl]- | 30158-52-2 | C14H12Cl2O2S |
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