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PHERECRATES , See also: Greek poet of the Old See also: Attic See also: Comedy, was a contemporary of See also: Cratinus, See also: Crates and Aristophanes
.
At first an actor, he seems to have gained a prize for a See also: play in 438 B.C
.
The only other ascertained date in his See also: life is 420, when he produced his play The See also: Wild Men
.
Like Crates, whom he imitated, he abandoned See also: personal satire for more general themes, although in some of the fragments of his plays we find him attacking See also: Alcibiades and others
.
He was especially famed for his inventive See also: imagination, and the elegance and purity of his diction are attested by the epithet arruccararos (most Attic) applied to him by See also: 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
.
See also: 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 hydrolyticSee also: dissociation in aqueous solution
.
When heated with concentrated hydrochloric acid the amino See also: group is replaced by the hydroxyl group and the phenolic eurhodols are produced
.
The symmetrical diaminophenazine is the See also: 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 See also: 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 See also: silk and mordanted See also: cotton a See also: fine See also: scarlet
.
It is known commercially as neutral red
.
For the phenazonium salts see See also: SAFRANINE
.
Phenazone is an isomer of See also: phenazine, to which it bears the same relation that phenanthrene bears to anthracene
.
It is formed by reducing diortho-dinitrodiphenyl with sodium See also: amalgam and methyl See also: alcohol, or by See also: 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
.
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