Chemistry Organic Building Blocks Sulfonates
Organosulfur chemistry defines a sulfonate as either a salt or ester of a sulfonic acid, characterized by the presence of the functional group R−S(=O)2−O−, wherein R represents an organic group.
Sulfonates can be described as the deprotonated or conjugate base forms of sulfonic acids.
Typically, sulfonates exhibit characteristics of stability in water, lack of oxidizing properties, and colorlessness.
As the conjugate base of sulfonic acid, sulfonates are highly acidic and exhibit rapid hydration. This property makes them a commonly used compound for surface functionalization.
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2-(2-(2,2,2-Trifluoroethoxy)phenoxy)ethyl methanesulfonate
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(S)-Oxiran-2-ylmethyl 3-nitrobenzenesulfonate
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tert-Butyl 3-(((trifluoromethyl)sulfonyl)oxy)-2,5-dihydro-1H-pyrrole-1-carboxylate
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S-Adenosyl-L-methionine disulfate tosylate
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4-(2-(4,4-Dimethyl-4,5-dihydrooxazol-2-yl)propan-2-yl)phenethyl 4-methylbenzenesulfonate
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2-(Thiophen-2-yl)ethyl 4-methylbenzenesulfonate
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(R,R)-1,2-Bis(Methanesulphonyloxymethyl)cyclohexane