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From carbon disulfide

Dinitrotoluene crystallizes in yellow needles from carbon disulfide and is soluble in a number of organic solvents. It is only slightly soluble in water, 0.03 g/100 g of water at 22°C. Its physical properties are Hsted in Table 13. [Pg.71]

Amino-4,6-dichlorophenol. This compound (11) forms long white needles from carbon disulfide, and aggregate spheres from benzene. It sublimes at 70—80°C (8 Pa = 0.06 mm Hg) and decomposes above 109 °C. It is freely soluble in benzene and carbon disulfide, and is sparingly soluble in petroleum ether, water, and ethanol. The free base is unstable and the hydrochloride salt (mp 280—285°C, dec) is employed commercially. [Pg.314]

For the most part, thiacyanocarbons are derived from "BAhr s Salt" [18820-77-4] (10), prepared from carbon disulfide and sodium cyanide (61) through the intermediacy of the sodium salt of carbonocyanidodithione acid [33498-03-2] C2NS2Na. [Pg.406]

The molecule S12, like Se, is of Dsd symmetry but in the soHd state it occupies sites of the much lower C211 symmetry [163]. Due to the low solubihty and the thermal decomposition on melting only solid state vibrational spectra have been recorded [2,79]. However, from carbon disulfide the compound Si2-CS2 crystallizes in which the S12 molecules occupy sites of the high Sg symmetry which is close to 03a [163]. The spectroscopic investigation of this adduct has resulted in a revision [79] of the earher vibrational assignment [2] and therefore also of the earlier force constants calculation [164]. In Fig. 24 the low-temperature Raman spectra of S12 and Si2-CS2 are shown. [Pg.73]

The complex also undergoes a variety of addition reactions with reagents such as methyl iodide, hydrochloric acid, benzoyl chloride, and allyl chloride.8 In a reaction similar to that of the decarboxylation of aldehydes, the complex will abstract CS from carbon disulfide to give the irans-thiocarbonyl complex rans-RhClCS[P(C8H6)5]2.9... [Pg.71]

Dithioacids have been generated from carbon disulfide with Grignard reagents or alkyl lithium at 0 °C. Subsequent treatment with sulfonamide in situ gives the corresponding both aliphatic as well as aromatic thioamides in 70-90% yields (Scheme 10).31... [Pg.150]


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Carbon disulfid

Carbon disulfide

Carbon disulfides

From disulfides

Ligands derived from carbon disulfide

Methane carbon disulfide from

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