Search results
Results from the WOW.Com Content Network
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 ...
Milk of sulfur (lac sulphuris) – formed by adding an acid to thion hudor (lime sulfur). Natron/soda ash/soda – sodium carbonate. Na 2 CO 3; Nitrum flammans – ammonium nitrate. Sugar of lead – lead(II) acetate, formed by dissolving lead oxide in vinegar. Thion hudor – lime sulfur, formed by boiling flowers of sulfur with slaked lime.
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.
potassium tetrachloroaluminate: 13821-13-1 AlCl 4 Na: sodium tetrachloroaluminate: 7784-16-9 AlCl 4 Rb: rubidium tetrachloroaluminate: 17992-02-8 AlCl 6 K 3: potassium hexachloroaluminate: 13782-08-6 AlCl 6 Na 3: sodium hexachloroaluminate: 60172-46-5 AlCo Alumanylidynecobalt: AlF: aluminium monofluoride: 13595-82-9 AlFO: aluminium monofluoride ...
Thus, cyclohexene, diiodomethane, and a zinc-copper couple (as iodomethylzinc iodide, ICH 2 ZnI) yield norcarane (bicyclo[4.1.0]heptane). [5] [6]The Simmons–Smith reaction is generally preferred over other methods of cyclopropanation, [7] however it can be expensive due to the high cost of diiodomethane.
Potassium hexafluorophosphate – KPF 6; Potassium hydrogen carbonate – KHCO 3; Potassium hydrogen fluoride – KHF 2; Potassium hydroxide – KOH; Potassium iodide – KI; Potassium iodate – KIO 3; Potassium manganate – K 2 MnO 4; Potassium monopersulfate – K 2 SO 4 ·KHSO 4 ·2KHSO 5; Potassium nitrate – KNO 3; Potassium perbromate ...
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.
Treatment of sulfur with hydrogen gives hydrogen sulfide.When dissolved in water, hydrogen sulfide is mildly acidic: [5] H 2 S ⇌ HS − + H +. Hydrogen sulfide gas and the hydrosulfide anion are extremely toxic to mammals, due to their inhibition of the oxygen-carrying capacity of hemoglobin and certain cytochromes in a manner analogous to cyanide and azide.