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Organosulfur chemistry is the study of the properties and synthesis of organosulfur compounds, which are organic compounds that contain sulfur. [1] They are often associated with foul odors, but many of the sweetest compounds known are organosulfur derivatives, e.g., saccharin. Nature is abound with organosulfur compounds—sulfur is vital for ...
In organosulfur chemistry, organosulfates are a class of organic compounds sharing a common functional group with the structure R−O−SO − 3. The SO 4 core is a sulfate group and the R group is any organic residue. All organosulfates are formally esters derived from alcohols and sulfuric acid (H 2 SO 4) although many are not prepared in ...
In organosulfur chemistry, S-oxide may refer to: S-oxides of disulfides, compounds with the linkage RSS(O)R. Several 1,2-dithiolanes for S-oxides. S-oxides of thioketones and thioaldehydes, compounds with the formula R 2 C=S=O and RCH=S=O, respectively. [1] syn-Propanethial-S-oxide, a lacrymatory component of onion, is one example.
In organic chemistry, a sulfide (British English sulphide) or thioether is an organosulfur functional group with the connectivity R−S−R' as shown on right. Like many other sulfur-containing compounds, volatile sulfides have foul odors. [1] A sulfide is similar to an ether except that it contains a sulfur atom in place of the oxygen.
Sulfolane (also tetramethylene sulfone, systematic name: 1λ 6-thiolane-1,1-dione) is an organosulfur compound, formally a cyclic sulfone, with the formula (C H 2) 4 S O 2.It is a colorless liquid commonly used in the chemical industry as a solvent for extractive distillation and chemical reactions.
In organosulfur chemistry, a Bunte salt is an archaic name for salts with the formula RSSO 3 – Na +. They are also called S-alkylthiosulfates or S-arylthiosulfates. [1] These compounds are typically derived from alkylation on the pendant sulfur of sodium thiosulfate: [2] [3] RX + Na 2 S 2 O 3 → Na[O 3 S 2 R] + NaX
In organosulfur chemistry, a sulfonate is a salt, anion or ester of a sulfonic acid. Its formula is R−S(=O) 2 −O −, containing the functional group −S(=O) 2 −O −, where R is typically an organyl group, amino group or a halogen atom. Sulfonates are the conjugate bases of sulfonic acids.
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