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Arylsulfonic Acids

Mocimycin has been chemically converted to aurodox by protection of the 4-hydroxy group at the pyridone moiety as the benzoylformate, followed by /V-methylation and hydrolytic removal of the protective group (1,55). Whereas aurodox esters are active growth promotors in animals, goldinamines that are A/-acylated by acids other than goldinonic acid, such as acetic, benzoic, or arylsulfonic acids, lack useful antimicrobial or growth-promoting activity (1). [Pg.524]

Fusion/Hydroxylation. The conversion of arylsulfonic acids to the corresponding hydroxy compound is normally effected by heating with caustic soda (caustic fusion). The primary examples are P-naphthol in the naphthalene series and resorcinol in the benzene series further examples are m- am in oph en o1 from metanilic acid and diethyl-y -arninophenol from /V,/V-diethy1metani1ic acid. In the naphthalene series the hydroxy group is much... [Pg.291]

Biedlingmeier JJ, A Schmidt (1983) Arylsulfonic acids and some 5-containing detergents as sulfur sources for growth of Chlorellafusca. Arch Microbiol 136 124-130. [Pg.79]

Imidazolides, 1,2,4-triazolides, or tetrazolides of arylsulfonic acids have been used as condensing agents in expedient syntheses of oligodeoxynucleotides. [Pg.265]

Instead of the isolated arylsulfonic acid azolides, mixtures of arylsulfonic acid chlorides and azoles have also been used for phosphorylation on a nucleoside 5 -OH or as coupling agents in the synthesis of oligodeoxyribonucleotides. 94 133 1371... [Pg.269]

Barium pigments, which are the barium salts of l-azo-2-hydroxy-naphthalenyl-arylsulfonic acid, are excluded from the generic classification of barium salts as harmful . This generic entry for barium salts mandates the labeling of other barium pigments, regardless of whether or not this would be required on the basis of experimental results [3]. [Pg.586]

Another concern for polystyrene- and some aromatic-based PEMs is hydrolysis of fhe sulfonic acid group from aromatic rings as well as hydrolytic cleavage of polymer backbone under fuel cell conditions for aromafic polymers including polyimides, poly(arylene ethers), poly(ether ketones), and poly(ether sulfones). It is well known that the sulfonation of aromafic rings is a reversible process especially at low pH and at elevated temperature (Scheme 3.3). The reversibility of sulfonation, for example, is used in fhe preparafion of trinitrotoluene or picric acid. Por the simplest membrane of the class of arylsulfonic acids (i.e., benzenesulfonic acid), fhe reacfion occurs upon freatment with a stream of superheated steam at 180°C.i ... [Pg.135]

Diazotization of 3,7-diaminodibenzothiophene 5,5-dioxide, which has the trivial name of benzidine sulfone, followed by coupling with phenols, anilines, or arylsulfonic acids gives bis-azo dyes varying in color from red-brown to blue. These dyes are useful for the coloring of plastics and cellulose. second class of compounds based on 3,7-diamino-... [Pg.266]


See other pages where Arylsulfonic Acids is mentioned: [Pg.120]    [Pg.121]    [Pg.123]    [Pg.125]    [Pg.127]    [Pg.129]    [Pg.131]    [Pg.133]    [Pg.135]    [Pg.137]    [Pg.139]    [Pg.141]    [Pg.598]    [Pg.251]    [Pg.268]    [Pg.135]    [Pg.264]    [Pg.13]    [Pg.139]    [Pg.140]    [Pg.142]    [Pg.144]    [Pg.146]    [Pg.148]    [Pg.150]    [Pg.152]    [Pg.154]    [Pg.156]    [Pg.158]    [Pg.160]    [Pg.585]    [Pg.1019]    [Pg.61]    [Pg.61]    [Pg.63]    [Pg.65]    [Pg.67]    [Pg.69]    [Pg.1019]    [Pg.180]   
See also in sourсe #XX -- [ Pg.761 ]

See also in sourсe #XX -- [ Pg.264 , Pg.265 ]

See also in sourсe #XX -- [ Pg.264 , Pg.265 ]

See also in sourсe #XX -- [ Pg.734 , Pg.755 ]




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