Organosulfonic acids and derivatives
Organosulfonic acids and their derivatives are a class of organic compounds that contain a sulfonic acid group (-SO3H) attached to an organic radical. These compounds play critical roles in various applications, including catalysis, pharmaceuticals, and surface chemistry.
In catalysis, organosulfonic acids function as powerful Lewis acids, facilitating chemical reactions by coordinating with reactants or activating transition metal catalysts. They are often used in the synthesis of fine chemicals, polymers, and other materials due to their strong acidity and electron-withdrawing nature.
Derivatives of these compounds include esters, amides, and salts, which can enhance their reactivity or stability depending on the application. For example, sulfonate esters are valuable intermediates in polymer synthesis and surfactant production, while sulfonamides find extensive use as drugs due to their ability to inhibit bacterial enzymes.
Overall, organosulfonic acids and their derivatives offer a versatile toolkit for researchers and industrial chemists seeking efficient solutions for complex chemical processes.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Lithium Bis(nonafluorobutanesulfonyl)imide | 119229-99-1 | C8F18LiNO4S2 |
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5-bromo-N-methanesulfonylpentanamide | 52533-64-9 | C6H12BrNO3S |
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| 59504-75-5 | C3H6BrNO3S |
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Methanesulfonamide,1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]-, potassium salt (1:1) | 90076-67-8 | C2HF6KNO4S2 |
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Carbamic acid, [(1-methylcyclopropyl)sulfonyl]-, 1,1-dimethylethyl ester | 849022-29-3 | C9H17NO4S |
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1,1,2,2,3,3,4,4,4-Nonafluoro-N-(2-methoxyethyl)-1-butanesulfonamide | 40630-68-0 | C7H8F9NO3S |
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Trihexyl(Tetradecyl)Phosphonium Bis(Trifluoromethyl)SulfonylAzanide | 460092-03-9 | C34H68F6NO4PS2 |
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Silver Bis(trifluoromethanesulfonyl)imide | 189114-61-2 | C2AgF6NO4S2 |
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Lithium bis(pentafluoroethanesulfonyl)imide | 132843-44-8 | C4F10LiNO4S2 |
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Trimethylpropylammonium Bis(trifluoromethanesulfonyl)imide | 268536-05-6 | C8H16F6N2O4S2 |
Related Literature
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Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
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Weili Dai,Guangjun Wu,Michael Hunger Chem. Commun., 2015,51, 13779-13782
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Domenico Lombardo,Gianmarco Munaò,Pietro Calandra,Luigi Pasqua,Maria Teresa Caccamo Phys. Chem. Chem. Phys., 2019,21, 11983-11991
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Matthew J. Gaunt,Jinquan Yu,Jonathan B. Spencer Chem. Commun., 2001, 1844-1845
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Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
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