When.com Web Search

  1. Ads

    related to: structural formula of sulfanilamide 3 oz glass bottles with swing top

Search results

  1. Results From The WOW.Com Content Network
  2. Sulfanilamide - Wikipedia

    en.wikipedia.org/wiki/Sulfanilamide

    Sulfanilamide (also spelled sulphanilamide) is a sulfonamide antibacterial drug. Chemically, it is an organic compound consisting of an aniline derivatized with a sulfonamide group. [1] Powdered sulfanilamide was used by the Allies in World War II to reduce infection rates and contributed to a dramatic reduction in mortality rates compared to ...

  3. Sulfinamide - Wikipedia

    en.wikipedia.org/wiki/Sulfinamide

    In organosulfur chemistry, sulfinamide is a functional group with the structure R−S(O)−NR 2 (where R = alkyl or aryl). [1] This functionality is composed of a sulfur - carbon ( S−C ) single bond , a sulfur- nitrogen ( S−N ) single bond , and a sulfur-oxygen (S-O) bond (see Sulfoxide for the nature of this bond) [ 2 ] .

  4. Sulfamide - Wikipedia

    en.wikipedia.org/wiki/Sulfamide

    In this example, the reactants are aniline, triethylamine (Et 3 N, Et = ethyl group), and iodine. Sulfur dioxide is believed to be activated through a series of intermediates: Et 3 N− + −I −, Et 3 N−I + −I − 3 and Et 3 N + −SO − 2. The sulfamide functional group is an increasingly common structural feature used in medicinal ...

  5. Structural formula - Wikipedia

    en.wikipedia.org/wiki/Structural_formula

    Skeletal structural formula of Vitamin B 12.Many organic molecules are too complicated to be specified by a molecular formula.. The structural formula of a chemical compound is a graphic representation of the molecular structure (determined by structural chemistry methods), showing how the atoms are connected to one another. [1]

  6. Sulfenamide - Wikipedia

    en.wikipedia.org/wiki/Sulfenamide

    Sulfenamides have been characterized by X-ray crystallography.The S-N bond in sulfenamides is a chiral axis that leads to formation of diastereomeric compounds. The existence of these distinct stereoisomers is due to the formation of a partial double bond between either sulfur or nitrogen's lone pair and the other atom's antibonding orbitals. [1]

  7. Acylsulfonamide - Wikipedia

    en.wikipedia.org/wiki/Acylsulfonamide

    Chemical structure of a generic acylsulfonamide. Acylsulfonamide is a functional group in organic chemistry that is sometimes used in medicinal chemistry. [1] It consists of a sulfonamide group (SO 2 NH) linked to an acyl group (RCO), forming the structure R 1-CO-NH-SO 2-R 2.