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  2. Sulfonamide - Wikipedia

    en.wikipedia.org/wiki/Sulfonamide

    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.

  3. List of compounds with carbon number 1 - Wikipedia

    en.wikipedia.org/wiki/List_of_compounds_with...

    chloro dibromo fluoro methane: 353-55-9 CBr 2 O: carbonyl bromide: 593-95-3 CBr 3: tribromomethyl radical: 4471-18-5 CBr 3 Cl: tribromochloromethane: 594-15-0 CBr 4: carbon tetrabromide: 558-13-4 CCe: cerium monocarbide: 12011-58-4 CCeRh: monocerium monorhodium monocarbide: 70378-91-5 CCeRu: monocerium monoruthenium monocarbide: 70378-92-6 ...

  4. Methanesulfonic acid - Wikipedia

    en.wikipedia.org/wiki/Methanesulfonic_acid

    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 ).

  5. Sulfonyl group - Wikipedia

    en.wikipedia.org/wiki/Sulfonyl_group

    Sulfonyl groups can be written as having the general formula R−S(=O) 2 −R′, where there are two double bonds between the sulfur and oxygen. [1]: 53 [2] Sulfonyl groups can be reduced to the sulfide with diisobutylaluminium hydride (DIBALH). Lithium aluminium hydride (LiAlH 4) reduces some but not all sulfones to sulfides. [1]: 1851

  6. Sulfonamide (medicine) - Wikipedia

    en.wikipedia.org/wiki/Sulfonamide_(medicine)

    Sulfonamide functional group Hydrochlorothiazide is a sulfonamide and a thiazide. Furosemide is a sulfonamide, but not a thiazide. Sulfamethoxazole is an antibacterial sulfonamide. Sulfonamide is a functional group (a part of a molecule) that is the basis of several groups of drugs, which are called sulphonamides, sulfa drugs or sulpha drugs.

  7. Methanesulfonyl azide - Wikipedia

    en.wikipedia.org/wiki/Methanesulfonyl_azide

    Methanesulfonyl azide melts at 18 °C and decomposes from 120 °C. [1] Like many other azides, it is explosive. [3] At low temperature, methanesulfonyl azide crystallizes in the triclinic crystal system in the space group P1 with the lattice parameters a = 5.6240 Å; b = 5.9498 Å, c = 7.6329 Å, α = 72.216°, β = 70.897°, and γ = 88.601°, and two molecules per unit cell.

  8. Methanesulfonyl chloride - Wikipedia

    en.wikipedia.org/wiki/Methanesulfonyl_chloride

    Methanesulfonyl chloride (mesyl chloride) is an organosulfur compound with the formula CH 3 SO 2 Cl. Using the organic pseudoelement symbol Ms for the methanesulfonyl (or mesyl) group CH 3 SO 2 –, it is frequently abbreviated MsCl in reaction schemes or equations. It is a colourless liquid that dissolves in polar organic solvents but is ...

  9. Bistriflimide - Wikipedia

    en.wikipedia.org/wiki/Bistriflimide

    Bistriflimidic acid. The conjugate acid of bistriflimide, which is frequently referred to by the trivial name bistriflimidic acid (CAS: 82113-65-3), is a commercially available superacid.