摘要:
Aryl-substituted perfluoroalkanesulfonanilides in which the aryl group comprises two optionally substituted phenyl rings linked by oxygen, and corresponding N-substituted compounds, are active herbicides and some are anti-inflammatory agents.
摘要:
Biphenyls substituted by a lower perfluoroalkylsulfonamido group and optionally containing lower alkyl, lower alkoxy, hydroxy, nitro, amino, halogen, alkanoyloxy, formamido, or phenyl substituents. These compounds and salts thereof are active as herbicidal and antimicrobial agents and are useful as polymer curing agents.
摘要:
Benzoylhaloalkanesulfonanilides having ring substituents selected from amino, nitro, carboxyl, mercapto, phenylsulfinyl, phenylsulfonyl, lower alkylsulfonamido, lower alkanoylamino, lower alkylthio, lower alkanoyloxy, lower alkylsulfamoyl, lower alkylsulfonoxy and lower haloalkylsulfonoxy. These compounds and salts thereof are active anti-inflammatory agents and some also have anti-pyretic and analgesic activity.
摘要:
NOVEL ALKALI METAL N-HALO-ALKANESULFONAMIDES, HAVING BLEACHING AND ANTISEPTIC PROPERTIES AND CAPABLE OF BEING FORMULATED IN BLEACHING AND DETERGENT COMPOSITIONS, ARE REPRESENTED BY THE FORMULATION
R-SO2-N(-X)-M
WHEREIN X IS CHLORINE OR BROMINE, M IS AN ALKALI METAL, AND R IS AN ALKYL HAVING FROM 1 TO ABOUT 22 CARBON ATOMS; THE NOVEL COMPOUNDS CAN BE PREPARED, FOR EXAMPLE, BY REACTING AN ALKANE SULFONAMIDE WITH AN ALKALI METAL HYPOCHLORITE OR HYPOBROMITE.
摘要:
Trifluoromethanesulfonamido-substituted desoxybenzoins and pharmaceutically acceptable salts thereof. These compounds are active anti-microbial agents.
摘要:
The invention provides compounds of the general formula (I) ##STR1## wherein Ar, R.sup.1, R.sup.2, X, Y and Q are defined in the specification and physiologically acceptable salts and solvates thereof.The compounds have a selective stimulant action at .beta..sub.2 -adrenoreceptors and may be used, inter alia, in the treatment of diseases associated with reversible airways obstruction such as asthma and chronic bronchitis.
摘要:
A 4-acyl-o-phenylenediamine is selectively sulfonated on the amino group meta to the acyl group to provide an important intermediate for benzimidazole pharmaceuticals. Some of the intermediates are new to organic chemistry.
摘要:
A process is provided which produces 3-sulfonylamino-4-aminobenzophenone intermediates useful in the regiospecific synthesis of benzimidazole antiviral agents.
摘要:
Cyclic sulfoperfluoroaliphaticcarboxylic acid anhydrides, amide derivatives thereof, a process for making the same, curable compositions containing cyclic sulfoperfluoroaliphaticcarboxylic acid anhydrides or amide derivatives thereof and cationically-sensitive monomers, and a process for using cyclic sulfoperfluoroaliphaticcarboxylic acid anhydrides or amide derivatives thereof as catalysts for the cure of cationically-sensitive monomers.