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Dimethyl sulfone (DMSO 2) is an organosulfur compound with the formula (CH 3) 2 SO 2. It is also known by several other names including methyl sulfone and (especially in alternative medicine) methylsulfonylmethane (MSM). [4] This colorless solid features the sulfonyl functional group and is the simplest of the sulfones. It is relatively inert ...
Methanesulfonic acid (MsOH, MSA) or methanesulphonic acid (in British English) is an organosulfuric, colorless liquid with the molecular formula CH 3 SO 3 H and structure H 3 C−S(=O) 2 −OH. It is the simplest of the alkylsulfonic acids ( R−S(=O) 2 −OH ).
Methanesulfonyl chloride is mainly used to give methanesulfonates by its reaction with alcohols in the presence of a non-nucleophilic base. [8] In contrast to the formation of toluenesulfonates from alcohols and p-toluenesulfonyl chloride in the presence of pyridine, the formation of methanesulfonates is believed to proceed via a mechanism wherein methanesulfonyl chloride first undergoes an ...
The general formula is R−SO 2 NR'R" or R−S(=O) 2 −NR'R", where each R is some organic group; for example, "methanesulfonamide" (where R = methane, R' = R" = hydrogen) is CH 3 SO 2 NH 2. Any sulfonamide can be considered as derived from a sulfonic acid by replacing a hydroxyl group (−OH) with an amine group.
Hydrogen: 0.2476 0.02661 Hydrogen bromide: 4.510 0.04431 Hydrogen chloride: 3.716 0.04081 Hydrogen cyanide [2] 11.29 0.0881 Hydrogen fluoride [2] 9.565 0.0739 Hydrogen iodide [2] 6.309 0.0530 Hydrogen selenide: 5.338 0.04637 Hydrogen sulfide: 4.490 0.04287 Isobutane [2] 13.32 0.1164 Iodobenzene: 33.52 0.1656 Krypton: 2.349 0.03978 Mercury: 8. ...
In organic chemistry, a methyl group is an alkyl derived from methane, containing one carbon atom bonded to three hydrogen atoms, having chemical formula CH 3 (whereas normal methane has the formula CH 4). In formulas, the group is often abbreviated as Me. This hydrocarbon group occurs in many organic compounds. It is a very stable group in ...
The acid was first unknowingly prepared in 1833 by Gustav Magnus as a decomposition product of ethanedisulfonic acid during early attempts [4] to synthesize diethyl ether from ethanol and anhydrous sulfuric acid by Magnus. [5] Early investigations focused on ether production from alcohols and strong anhydrous acids.
The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.