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Sulfonic acid amides amines

Sulfonylamines s. Disulfonyl-amines. Sulfonic acid amides, Trisulfonylamines Sulfonylamino groups, derivatives s. Trichlorophosphazo-sulfonyl compounds Sulfonylaminophenols... [Pg.332]

The dynamic thiolester system was subsequently expanded by incorporating three additional thiols in order to probe the performances of the thiol moiety to the target enzyme as well as the enzyme selectivity. Three thiols, 8, 10, and 12, having different adjacent functionalities, amine, sulfonic acid, and amide, respectively, were chosen and added to the dynamic thiolester system. The thiols were chosen due to their solubilities in aqueous media at neutral pH, and also for having similar exchange rates with acetylthiocholine. The kinetic and thermodynamic behavior of thiols/thiolesters are dependent on their structure and functionality,... [Pg.61]

Successful partition chromatography requires a proper balance of intermolecular forces among the three participants in the separation process—the analyte, the mobile phase, and the stationary phase. These intermoleculai forces are described qualitatively in terms of the relative polarity possessed by each of the three components. In general, the polai ities of common organic functional groups in increasing order are aliphatic hydrocarbons < olefins < aromatic hydrocarbons < halides < sulfides < ethers < nitro compounds < esters = aldehydes = ketones < alcohols = amines < sulfones < sulfoxides < amides < carboxylic acids < water. [Pg.984]

Although perfluorocarbon sulfonic acid groups are very stable chemically as well as thermally, perfluorocarbon sulfonyl halide, especially sulfonyl chloride groups, are quite reactive. For example, sulfonyl chloride groups react with oxidants, reductants, various amines, phenol compounds, iodine compounds, etc. and give carboxylic acid, sulfinic acid, sulfonic acid amide, -CF2I and so forth. Some examples of how this feature can be used to generate various kinds of membranes will next be described... [Pg.408]

See. from prim, amines via sulfonic acid amides... [Pg.131]

Amines from thiourethans N-Detosylation s. a. Amines from sulfonic acid amides —, oxidative 20, 562 suppl. 20 —, preferential 16, 367 0-Detosylation of nucleosides 18, 8... [Pg.312]

Sulfonic acid amides from sulfonic acid hydrazides Amines from hydrazones... [Pg.19]

Cupric acetate Amines from chlorides via sulfonic acid amides Preferential replacement of halogen... [Pg.122]

Sulfuric acid acetic acid Amines from sulfonic acid amides s. 5,28 s. a. P. D. Carpenter and M. Lennon, Chem. Commun. 1973, 664... [Pg.18]

A. for fibers ( textile auxiliaries) are sulfonates and phosphates, - fatty amines, - fatty acid amides and their ethoxylates, - quaternary ammonium compounds as well as - fatty alcohol ethoxylates, fatty acid esters and their derivatives. For more durable finishes, polyamine resins cross-linked on the fiber are used. [Pg.15]

Other Applications. Hydroxylamine-O-sulfonic acid [2950-43-8] h.2is many applications in the area of organic synthesis. The use of this material for organic transformations has been thoroughly reviewed (125,126). The preparation of the acid involves the reaction of hydroxjlamine [5470-11-1] with oleum in the presence of ammonium sulfate [7783-20-2] (127). The acid has found appHcation in the preparation of hydra2ines from amines, aUphatic amines from activated methylene compounds, aromatic amines from activated aromatic compounds, amides from esters, and oximes. It is also an important reagent in reductive deamination and specialty nitrile production. [Pg.103]


See other pages where Sulfonic acid amides amines is mentioned: [Pg.399]    [Pg.399]    [Pg.173]    [Pg.359]    [Pg.160]    [Pg.89]    [Pg.140]    [Pg.255]    [Pg.10]    [Pg.1037]    [Pg.17]    [Pg.76]    [Pg.134]    [Pg.95]    [Pg.259]    [Pg.291]    [Pg.509]    [Pg.711]    [Pg.172]    [Pg.251]    [Pg.283]    [Pg.763]    [Pg.948]    [Pg.372]    [Pg.174]    [Pg.48]   
See also in sourсe #XX -- [ Pg.11 ]




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Amide sulfon

Amides amines

Amides sulfonated

Amination/amidation

Amination/amidation Amines

Amine oxides sulfonic acid amides

Amines acid sulfonation

Sulfonic acid amides

Sulfonic acid amides sulfonates

Sulfonic acid amides sulfones

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