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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. Methyl methanesulfonate - Wikipedia

    en.wikipedia.org/wiki/Methyl_methanesulfonate

    Methyl methanesulfonate (MMS), also known as methyl mesylate, is an alkylating agent and a carcinogen. It is also a suspected reproductive toxicant, and may also be a skin/sense organ toxicant. [ 1 ] It is used in cancer treatment.

  4. N-Methylformamide - Wikipedia

    en.wikipedia.org/wiki/N-Methylformamide

    N-Methylformamide (NMF) is a colorless, nearly odorless, organic compound and secondary amide with molecular formula CH 3 NHCHO, which is a liquid at room temperature. NMF is mainly used as a reagent in various organic syntheses with limited applications as a highly polar solvent .

  5. 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 ).

  6. Bis(trifluoromethanesulfonyl)aniline - Wikipedia

    en.wikipedia.org/wiki/Bis(trifluoromethanesulfo...

    Bis(trifluoromethanesulfonyl)aniline is the organic compound with the formula C 6 H 5 N(SO 2 CF 3) 2. [1] It is a white solid. The compound is used to install the triflyl group (SO 2 CF 3 ).

  7. N-Nitrosodimethylamine - Wikipedia

    en.wikipedia.org/wiki/N-Nitrosodimethylamine

    The C 2 N 2 O core of NDMA is planar, as established by X-ray crystallography. The central nitrogen is bound to two methyl groups and the NO group with bond angles of 120°. The N-N and N-O distances are 1.32 and 1.26 Å, respectively. [14] NDMA forms from a variety of dimethylamine-containing compounds, e.g. hydrolysis of dimethylformamide.

  8. Bistriflimide - Wikipedia

    en.wikipedia.org/wiki/Bistriflimide

    The name 1,1,1-trifluoro-N-((trifluoromethyl)sulfonyl)methanesulfonamide is also an unambiguous IUPAC-acceptable name, though the symmetry of the molecule is not apparent from this construction. See also

  9. Methylsulfonylmethane - Wikipedia

    en.wikipedia.org/wiki/Methylsulfonylmethane

    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 chemically and is able to resist decomposition at elevated temperatures.