Dichloroacetic acid phenyl

D1CHLORO-5-PHENYL ISOCYANATE DICHLOROACETIC ACID DICHLOROACETYL CHLORIDE DICHLOROANILINE... [Pg.215]

Iodopropene Iodotoluene, 3- and 4-Isobutylbenzene Isobutyl dichloroacetate Isobutyl phenyl ketone Isobutyl trichloroacetate Isobutyronitrile Isopropyl acetate Isopropylbenzene Isopropyl nitrate Isopropyl trichloroacetate Isothiocyanic acid... [Pg.622]

It is important to know that nature can make a myriad of compounds with such xenobiotic bonds. See, for instance, Grimvall (1995) and Hjelm (1996). Good examples are the antibiotic called chloramphenicol and the hormone thyroxin. The former is an amide of dichloroacetic acid. Chloramphenicol has a nitrophenyl group, which is very rare in biological molecules. Thyroxin has an iodinated phenyl group. [Pg.216]

The kinetics and mechanism of the decarboxylation of 5- (p-substituted phenyl )-2-oxazolecarboxylic acids in neutral, acidic, and basic media have been studied by Tanaka.392 In quinoline or in dichloroacetic acid as a nonaqueous solvent, the reaction shows first-order kinetics.392 Studies on the decarboxylation of oxazolium (and other related azolium) carboxylates indicate that both 2- and 5-acids decarboxylate through their zwitterionic tautomers.393 Heating an oxazole-2-carboxylic acid at or above its melting point may also result in decarboxylation.29 394... [Pg.202]

See under Dichl phenylhydrazine. a o-Dichlorophsnylacetic Acid [Phenyl-dichloroacetic acid)... [Pg.781]

Poly(urethane)with methylene hir(4-phenyl isocyanate), ti Dimethylacetamide Dichloroacetic acid Sulfuric acid (90"/o)... [Pg.1515]

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