Online Encyclopedia

PHERECRATES

Online Encyclopedia
Originally appearing in Volume V21, Page 365 of the 1911 Encyclopedia Britannica.
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PHERECRATES  ,

Greek poet of the Old Attic
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Comedy, was a contemporary of Cratinus,
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Crates and Aristophanes . At first an actor, he seems to have gained a prize for a
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play in 438 B.C . The only other ascertained date in his
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life is 420, when he produced his play The Wild Men . Like Crates, whom he imitated, he abandoned
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personal satire for more general themes, although in some of the fragments of his plays we find him attacking Alcibiades and others . He was especially famed for his inventive
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imagination, and the elegance and purity of his diction are attested by the epithet arruccararos (most Attic) applied to him by
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Athenaeus and the sophist Phrynichus . He was the inventor of a new metre, called after him Pherecratean, which frequently occurs in the choruses of Greek tragedies and in Horace . A considerable number of fragments from his 16 (or . 13) plays has been preserved, collected in T . Kock, Comicorum Atticorum Fragmenta, i . (188o), and A . Meineke, Poetarum Comicorum Graecorum Fragmenta (1855) . Para position, or by oxidizing ortho-hydroxydiaminodiphenylamines (R .

Nietzki, Ber., 1895, 28, p . 2976; 0 .

Fischer, ibid., 1896, 29, I p . 1874) . They are yellowish-red solids, which behave as weak bases, their salts undergoing hydrolytic
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dissociation in aqueous solution . When heated with concentrated hydrochloric acid the amino
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group is replaced by the hydroxyl group and the phenolic eurhodols are produced . The symmetrical diaminophenazine is the parent substance of the important dyestuff toluylene red or dimethyldiaminotoluphenazine . It is obtained by the oxidation of orthophenylene diamine with ferric chloride; when a mixture of para-aminodimethylaniline and
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meta-toluylenediamine is oxidized in the cold, toluylene blue, an indamine, being formed as an intermediate product and passing into the red when boiled; and also by the oxidation of dimethylparaphenylene diamine with metatoluylene diamine . It crystallizes in orange-red needles and its alcoholic solution fluoresces strongly . It dyes
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silk and mordanted cotton a
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fine
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scarlet . It is known commercially as neutral red . For the phenazonium salts see
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SAFRANINE .

Phenazone is an isomer of

phenazine, to which it bears the same relation that phenanthrene bears to anthracene . It is formed by reducing diortho-dinitrodiphenyl with sodium
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amalgam and methyl
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alcohol, or by
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heating diphenylene-ortho-dihydrazine with hydrochloric acid to 15o° C . It crystallizes in needles which melt at 156° C . Potassium permanganate oxidizes it to pyridazine tetra-carboxylic acid . or (X:\/~//) N: \ Phenazine . Phenazone .

End of Article: PHERECRATES
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