Carbon disulfide Benzene

Ethylene Cyanohydrin. This cyanohydrin, also known as hydracrylonitnle or glycocyanohydrin [109-78-4] is a straw-colored Hquid miscible with water, acetone, methyl ethyl ketone, and ethanol, and is insoluble in benzene, carbon disulfide, and carbon tetrachloride. Ethylene cyanohydrin differs from the other cyanohydrins discussed here in that it is a P-cyanohydrin. It is formed by the reaction of ethylene oxide with hydrogen cyanide. 

Compounds with low flash points (below room temperature). Examples are acetaldehyde, acetone, acetonitrile, benzene, carbon disulfide, cyclohexane, diethyl ether, ethyl acetate and -hexane. 

Petroleum ether with acetic acid, acetone, benzene, carbon disulfide or diethyl ether. 

Organic solvent(s) Partition coefficients Soluble in ether, benzene carbon disulfide, alcoholb No data Soluble in alcohol, benzene, ether15 soluble in acetic acidg... 

Coking Multiple ammonia, benzene, carbon disulfide, carbon monoxide, cyanamides, hydrogen... 

Brillouin scattering of laser light in liquids has been studied by several authors. Shapiro etal. 233) measured hypersonic velocities in various liquids and obtained a Brillouin linewidth of 0.011 cm" in methylene chloride but of less than 0.002 cm in benzene, carbon disulfide and chloroform. The broadening of the Brillouin components arises from damping of thermal phonons and is closely connected with the viscosity coefficient of the medium. From the measured linewidths, the lifetimes of the phonons responsible for Brillouin scattering at 89 45 were calculated to be 4.8 x 10 sec for methylene chloride and 7.6 x 10 sec for toluene. 

Isomerically pure chlorofullerene C oClg has been reported to be the predominant product of the reaction of with an excess of iodine monochloride in benzene or toluene at room temperature (Scheme 9.11) [79], The product is very soluble in benzene, carbon disulfide and tetrachloromethane. Deep orange crystals can be obtained by recrystallization from pentane. The synthesis of CjoClg using toluene as a solvent proceeds more slowly than with benzene, indicating that radicals are involved and are scavenged by the toluene [79],... 

Dark red, fuming liquid reddish yellow vapors musty buring odor density 1.91 g/mL freezes at -96.5°C boils at 117°C reacts with water soluble in chloroform, carhon tetrachloride, benzene, carbon disulfide and nitrobenzene. 

Colorless fuming liquid pungent odor refractive index 1.516 at 14°C density 1.574g/mL at 21°C hods at 76°C freezes at -112°C decomposes in water soluble in benzene, carbon disulfide, ether and chloroform and other halo-genated organic solvents. 

Solubility. Decomposes in water and ethanol soluble in benzene, carbon disulfide and carbon tetrachloride miscible with diethyl ether (Budavari, 1996) Vapour pressure-. 53 Pa at 20°C relative vapour density (air = 1), 4.88 (Verschueren, 1996)... 

Benzoyl chloride, [98-88-4], C6HbCOC1 (mp, — 1°C bp, 197.2°C at 101.3 kPa d2B/4, 1.2070 r][, 1.55369), is a colorless liquid that fumes upon exposure to the atmosphere. It has a sharp odor and, in vapor form, is a strong lachrimator. It is decomposed by water and alcohol, and is miscible with ether, benzene, carbon disulfide, and oils. 

Soluble in Alcohol, carbon disulfide, chloroform, ether, mmiscible in water Benzene, carbon disulfide, chloroform, ether. Slightly form, soluble in alcohol. Carbon disulfide, chloroform, ether, petroleum ether. Insoluble in alkalies, but saponified by alkali hydroxides with formation of soaps. Slightly soluble in alcohol. Insoluble in water. Alcohol, carbon disulfide, chloroform, ether. Insoluble in water. ... 

Soluble in Benzene, carbon disulfide, Alcohol, carbon disulfide, Alcohol, carbon disulfide, ... 

Almost insoluble in water freely soluble in aqueous solutions of iodide. Soluble in benzene, carbon disulfide, ethanol, ethyl ether, cycohexane, carbon tetrachloride, chloroform, glacial acetic acid, and glycerol oils.1... 

The low-frequency feature in the reduced spectral density corresponds to the long-time tail of the intermolecular response function, which is often denoted the intermediate response in the OKE literature (15,51). In most liquids, this portion of the response appears to be exponential over a significant time scale. Why this portion of the response is exponential and what information the time scale of this exponential holds is still poorly understood. For this reason, we have performed detailed temperature-dependent studies of the intermediate relaxation in six symmetric-top liquids acetonitrile, acetonitrile-d3, benzene, carbon disulfide, chloroform, and methyl iodide (56). 

Attempts should be made to use alternate solvents for industrial processes. Solvents that pose and cause the most serious risk to human health should be replaced by less hazardous ones. If this is not possible, at least the work conditions and exposure to solvents should be adjusted to avoid or minimize the health risk. This may be achieved, for example, by using a closed process. Among solvents, the most hazardous ones identified are benzene, carbon disulfide, and carbon tetrachloride. 

The properties of niobium (V) chloride are well known. Cesium hexachloroniobate(V) is a bright yellow, crystalline, moisture-sensitive compound. It is soluble in iodine (I) chloride, less so in iodine (I) chloride-thionyl chloride mixtures, and completely insoluble in thionyl chloride it is very slightly soluble in acetonitrile and nitromethane but insoluble in benzene, carbon disulfide, ethyl acetate, and diethyl... 

Salts are insoluble in most solvents. Gasoline, benzene, carbon disulfide (CS ), carbon tetrachloride (CCl ), alcohol, ether—these substances are good solvents" for grease, rubber, organic materials generally but they do not dissolve salts. 

Addition of polycyclic aromatic hydrocarbons across the N(3)-C(4) bond of quinazoline takes plaee when equimolar amounts of the reactants are treated in an inert solvent (e.g., benzene, carbon disulfide, chloroform) with an excess of trifluoroacetic acid. The yields range from 60 to more than 90%. ... 

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